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The Opportunity: * The Procurement Category Lead is responsible for the developing and execution of Strategic Sourcing Strategies for Indirect goods and/or services within a defined portfolio of CSL Enterprise wide spends. * The I&T lead will be accountable for securing maximum value from the external spend of $450M+, from our suppliers and creating competitive advantage for CSL by delivering year on year multi-million-dollar savings, mitigation of associated risks, implementing supplier relationship management, identifying and delivering innovation and protecting CSL through robust contractual negotiations. * This role is seen as the Global SME for categories such as Hardware, Software, Data Centers, IT maintenance, licenses etc and is responsible for creating appropriate senior level stakeholder engagement & alignment plans to ensure the current and future needs of the business are addressed. * You will provide guidance to the Sourcing Managers within the team. This role will be directly involved in major global sourcing activities, driving key transformational projects, and building and maintaining relationships with key senior stakeholders internal to CSL Group and within large, external global vendors to bring leading edge and best practice innovation back into CSL to drive year on efficiency improvements. The Role: * Procurement Category Strategy & Development- * Develop and implement annual action plans for relevant categories based on the Procurement Strategy and other relevant business strategies within CSL to ensure clear objectives and action plans for Global Category Management Lead roles resulting in the reduction of the total cost of ownership and risk, while increasing innovation, customer service, compliance, and quality. * Focus on the development of operational plans in conjunction with the respective business unit with a strategic long-term focus of future operating models or processes over the next 3 -5 years. * Take a leadership position and drive collaborate with the respective business unit on complex problem resolution, investigative data analytics, process reengineering and establishment of a sustainable program that will fill a global need while being consistent within all Company areas affected. * Analyze spend, market trends and supply risks to effectively manage procurement activities to ensure cost efficiency and optimal supplier performance. * Provide strategic direction and operational support to Sourcing Managers to execute procurement activities * Lead, motivate and develop employees within the Procurement organization including effective long-term talent development, succession planning and performance managing with a focus on supporting employees to meet or exceed performance expectations while demonstrating CSL Values. * Supplier relationship management- * Drive value from the global category(s) by defining and implementing effective strategy category management; establishing and managing Councils for business-critical commodities aligned with the evolving business requirements and are effectively leading key sourcing activities, including negotiations, that to deliver lower cost of ownership, lower risk, higher quality, and better supply performance across the short and long term. * Facilitate supplier business performance reviews and ensure alignment with contractual and CSL needs and priorities and establish supplier performance management (KPIs, scorecards, reviews) to drive year on year improvements * Lead supplier risk management and continuity planning within the categories of responsibility. * Lead complex and business negotiations with major key suppliers and provide advice for regional sourcing as required. * Develop long term strategies to ensure supplier sustainability and continuity while implementing a partnership with the supplier to drive year over year continuous improvement * Conduct business with integrity, in accordance with the highest ethical standards and in compliance with all applicable laws and regulations and anti-bribery requirements and supports diversity and inclusion by promoting utilization of small, disadvantaged and/or diverse suppliers. * Ensure that Conflicts of Interest are not present with supplier selection and the sourcing process is free from all potential Conflicts of Interest. * Execute sourcing and procurement activities- * Engage with internal stakeholders across CSL to align procurement initiatives and saving opportunities. * Ensure compliance with procurement policies and governance frameworks and ethical sourcing standards * Maintain accurate documentation and reporting of procurement activities and supplier engagements. * Monitor category performance using key performance indicators (KPIs) and provide insights to facilitate better, faster decisions to the Category Director and key stakeholders across Commercial and Finance. * Identify and manage procurement-related risks within assigned categories. * Lead the Tendering process, negotiations, and contract awards for activities over $500K. * Drive total cost of ownership (TCO) improvements, cost reduction, and value creation. * Stakeholder Collaboration - * Build and maintain effective professional relationships with senior, internal stakeholders and senior external executives within large vendors to deliver upon Procurement’s objectives by ongoing discussions and participation in formal teams and groups with senior leaders in CSL and external vendors to manage supplier performance, issues, procurement improvement initiatives and other broader business issues. * Partner with internal stakeholders (I&T, Finance, Legal, etc.) to translate business requirements into sourcing and contracting strategies. * Act as the primary procurement point of contact for assigned categories. * Cost analysis and budget management - * Conduct detailed cost analysis and benchmarking to identify savings opportunities and ensure procurement activities align with financial objectives. * Monitor and report category performance against budget using KPIs and data-driven insights to support cost optimization and compliance. Additional Responsibilities: * Risk management. * Training and development. * Market intelligence sharing. * Support change initiatives. * Stakeholder engagement. Skills & Experience: * Bachelor’s degree in Procurement / Supply Chain Management preferred or related field * Post graduate business degree, MBA highly regarded * Minimum 7+ years’ experience in procurement, sourcing, or category management roles. * Demonstrated success in developing category strategies and managing supplier relationships. * Experience in performance monitoring, risk management, and cross-functional collaboration. * Experience of multi-site organizations. * Ability to develop and implement long-term category strategies that align with organisational objectives and drive measurable value. * Expertise in building and maintaining strong relationships with suppliers to enhance collaboration and performance. * Ability to turn insights into action and make decisions based on data and analysis provided by the COE. * Strong negotiation abilities to secure favourable terms and conditions. * Ability to work effectively with internal stakeholders across various departments to ensure alignment on procurement initiatives. * Ability to work across time zones and manage global stakeholder relationships * Travel Requirements (Domestic, International, frequency) - 20% travel expected CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives. CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries. To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit ___ and CSL Plasma at ___. Our Benefits For more information on CSL benefits visit ___. You Belong at CSL At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. To learn more about inclusion and belonging visit Equal Opportunity Employer CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit ___.

CSL's organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, we’re building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide. Could you be our next Associate Director, Data Science & AI? The job is in our King of Prussia, PA Office. This is a hybrid position and is onsite three days a week. You will report to the Senior Director of Commercial Business Analytics. About The Role We are seeking a visionary and strategic leader to spearhead the development and commercialization of (Gen) AI solutions tailored for the life sciences industry. The Insights and Analytics team is dedicated to enabling improved decision making at CSL by leveraging superior data to identify actionable insights that drive enhanced performance. We collaborate closely with the US & International business, bringing insights and challenging ideas to empower smarter, data-driven decision-making. You will spearhead the application of advanced analytics, machine learning, and AI solutions to unlock new insights, accelerate decision-making, and enhance commercial outcomes across CSL Behring’s portfolio. You will focus on embedding AI and predictive modeling into core commercial processes, including patient identification, Medical and Tender Analytics, forecasting, and customer insights. in this role, you will serve as a bridge between CSL’s commercial business needs and technical innovation, ensuring scalable and responsible use of AI to create measurable business impact. The ideal candidate brings deep domain expertise, a strong innovation mindset, and a proven track record of translating AI capabilities into impactful business solutions. Major Responsibilities * Lead development and deployment of advanced analytics and AI models to address critical commercial challenges (patient identification in rare disease, HCP segmentation, Medical and Tender use cases) * In close partnership with ABCIA Commercial, Medical Affairs, and Market Access teams to ensure solutions are aligned with strategic business needs * Translate business problems into well-defined data science use cases and develop proof-of-concept pilots through to production * Drive adoption of AI-enabled tools across the commercial organization, ensuring business users understand and trust the outputs * Partner with I&T and Data Governance to ensure responsible AI practices, data quality, and scalable infrastructure * Drive CSL innovation in the field, leading to high visibility publications in top AI conferences and patents around Generative AI, reasoning, multi-agent systems, etc * Establish KPIs and frameworks to measure ROI and business impact of data science projects * Stay current with emerging AI/Machine Learning (ML)techniques, tools, and regulatory developments, and translate those into CSL’s context * Develop strong external partnerships (vendors and external partners) to bring cutting-edge AI capabilities into CSL and represent Commercial Data Science in cross-functional governance forums, ensuring alignment with global AI/ML initiatives Qualifications * Bachelor’s in data science, AI, Computer Science, Statistics, Applied Mathematics, or related quantitative discipline. Master’s degree preferred * 10+ years of experience in advanced analytics, data science, or (Gen)AI within pharma/biotech or healthcare; commercial analytics experience strongly preferred. * Strong track record of developing and deploying machine learning models in commercial or clinical contexts. Strong analytical and problem-solving skills, with the ability to interpret complex data and make informed decisions * A deep understanding of the pharmaceutical industry, including regulatory requirements, market dynamics, and emerging AI technologies, with the foresight to identify and map both current and future AI opportunities, is preferred. * Experience leading cross-functional AI/ML initiatives from concept through deployment. * Familiarity with cloud environments (AWS and Snowflake), data engineering workflows, and modern ML frameworks (TensorFlow, PyTorch, scikit-learn) and familiarity with no-code data science SaaS tools * Develop strong external partnerships (vendors and external partners) to bring cutting-edge AI capabilities into CSL and represent Commercial Data Science in cross-functional governance forums, ensuring alignment with global AI/ML initiatives * Ability to adapt strategies and approaches in a rapidly evolving technological landscape Additional Qualifications – Preferred * Experience in rare disease patient-finding models a plus. * Experience building evaluation frameworks for LLMs (factuality, faithfulness, bias, toxicity) and human-in-the-loop review * Knowledge of responsible AI frameworks, data governance, and compliance in pharma settings. Experience Leading design, training/fine-tuning, and evaluation of ML/LLM/Agentic systems (retrieval-augmented generation, tool-use, routing, multi-agent workflows). #LI-HYBRID CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives. CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries. To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit ___ and CSL Plasma at ___. Our Benefits For more information on CSL benefits visit ___. You Belong at CSL At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. To learn more about inclusion and belonging visit Equal Opportunity Employer CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit ___.

Job Description CSL's organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, we’re building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide. Could you be our next Associate Director, Medical Grants and IIS Operations? The job is in our King of Prussia, PA or Waltham, MA Office. This is a hybrid position and is onsite three days a week. You will report to the Director Head of Global Medical, Grants & IIS Operations. You will partner closely with the Director for Grants & IIS to redesign the grants intake and approval process to allow for end-to-end enterprise approach across all grant activities. The role will be responsible for supporting strategic evaluation of all grants applications, ensuring compliant review and processing of grants, and liaising with finance stakeholders to maintain compliance and alignment with budget. You will support the Director in evaluating, tracking, and closing out IISs in close alignment with disease area leads. Based on an excellent understanding of the legal and regulatory requirements, the position will ensure that policies reflect the highest levels of ethics and compliance, that review of applications is based solely on scientific merit and alignment with prespecified scope, decisions are communicated in a timely manner, and that subsequent contracting and milestones are accomplished seamlessly. Main Responsibilities and Accountabilities: • Responsible for oversight of an end-to-end enterprise approach to grants to ensure a rigorous framework for strategic decision-making consistently across geographies, • Responsible for ensuring all grants and IIS applications are processed through CyberGrants (or designated platform), • Leads Grants Review Committees, ensuring that all required voting members are present at each meeting, and that the outcomes of each meeting are documented., • Responsible for the governance, development of an industry-leading Grants program and challenging the status quo with continuous improvement of Grants and for providing subject matter expertise to ensure Medical colleagues globally are fully trained on process, • Accountable to provide regular impact metrics of approved and ongoing grants, including milestones, • Responsible for the governance and oversight of grants in Medical Affairs in CyberGrants (or designated platform)., • Provide additional leadership to the broader team by having a positive, solutions-focused, innovative and collaborative mindset, • Provide support to IIS activities as needed Qualifications: • Bachelor’s Degree required or MD/PharmD/PhD equivalent experience, advanced degree preferred., • 10+ years of pharmaceutical/biotherapeutics industry experience, • Experience in drug safety, pharmacovigilance, quality assurance and compliance requirements are desirable, • 3+ years of Medical Affairs Leadership experience, • Experience in biomedical research, study feasibility #LI-HYBRID About CSL Behring CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives. CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries. To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit ___ and CSL Plasma at ___. Our Benefits For more information on CSL benefits visit ___. You Belong at CSL At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. To learn more about inclusion and belonging visit Equal Opportunity Employer CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit ___.

The Associate Director of Business Analytics US I&A is data and analytics leader in support CSL‘s brand teams with strategic insight through quantitative analytics and reporting. The role is to guide the Business Team to proactively plan, design and lead initiatives for in-line and launch products. Contribute to the development of portfolio and brand strategy development through understanding the quantitative and qualitative market context and CSL Behring’s strategic opportunities. Develop metrics, KPI Dashboards, and other tools to quantify key performance indicators that connect strategic intent with tactical execution. The role will serve as the subject matter expert on healthcare data and will coach & mentor other analysts/Managers on use/best practices. The incumbant will take a leadership role in making CSL Behring more responsive to market changes driven by consumer needs and competitive dynamics. With strong business acumen, this role must be able to integrate and cross analyze both quantitative and qualitative information from multiple sources into a comprehensive evaluation with well supported recommendations that are relevant, timely and actionable. An entrepreneurial mindset and a drive to grow with the position are most important success factors. Responsibilities • As a leader in business analytics team proactively plan, manage and execute commercial data modeling and scenario analysis using a mix of competitive intelligence, secondary and primary research techniques as needed., • Deliver high quality, timely and actionable insights that characterize opportunities and risks and translate into clear management recommendations with associated implications for the business., • As a technology leader in manage & support enterprise analytical projects, platform development, data acquisitions, analytical vendor relationships, Omnichannel etc.., • Decision support using a broad range of quantitative techniques to analyze, interpret and understand main business and market dynamics. Present detailed quantitative analysis and qualitative insights to senior leadership in a manner that is easily interpreted and aids strategic decision-making., • Operate as a business partner to CSL Behring brand teams through provision of research and analysis to provide quantitative market, competitor and brand insights.Build a working relationship with US Market Research & CI leads to develop a deeper understanding of patient dynamics, competitive landscape to proactively identify growth opportunities for CSL US portfolio., • Partner with external vendors to initiate secondary data research to identify the barriers and opportunities for demand generation in CSL brands., • For assigned projects, monitor, control, and negotiate all research & analytics related expenses to ensure the cost-effective use of resources., • Strong business acumen & presentation skills to senior leadership to aid & influence the data driven decision making. Qualifications • Bachelors degree with quantitative focus required (engineering, statistics, mathematical sciences, economics). Master’s Degree preferred, • 8 to 10 years’ professional experience with a focus on quantitative analysis and decision support., • Advanced Knowledge of Pharmaceutical data including but not limited to IQVIA Claims, DDD, Symphony Non Retail, SP Claims, • Prior commercial analytics experience in Rare diseases, oncology , novel therapies or Biotech is a huge plus., • Prior experience in management consulting, Brand analytics, patient analytics or Market Access analytics or equity research analysis. Different qualifications or responsibilities may apply based on local legal and/or educational requirements. Refer to local job documentation where applicable. CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives. CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries. To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit ___ and CSL Plasma at ___. Our Benefits For more information on CSL benefits visit ___. You Belong at CSL At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. To learn more about inclusion and belonging visit Equal Opportunity Employer CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit ___.

The Associate Director (AD), Biostatistics, leads the full scope of statistical contribution to a clinical development program. The AD provides statistical strategies for the clinical trials and regulatory submissions, and is accountable for the statistical deliverables within the program. 1 Lead full scope of Biostatistics conduct for the responsible program within a therapeutic area. Define statistical strategy and ensure appropriate statistical methodologies applied to study design and data analysis for clinical trials and regulatory submissions 2 Influence and contribute to clinical development plans, collaborate with cross-functional team for governance reviews. Lead statistical strategy for planning and study execution (member of Study Executive Team, Clinical Development Team) and quantitative evaluation to clinical trials, regulatory submissions, and related documents. 3 Provide statistical thought partnership for innovative study design and clinical development plans, including Go-No Go criteria and probability of technical success calculations. 4 Provide for project-wide planning of analyses; quality and timely delivery of interim and final results, including integrated analyses for submissions. 5 Represent Biostatistics in interactions with regulatory authorities (eg, FDA, EMA, PMDA) 6 Be responsible for interpreting analysis results and ensuring reporting accuracy in study reports and regulatory documents. 7 Manage outsourcing operations or work with internal statistical programmers within the responsible program. Ensure timeliness and quality of deliverables by CRO/FSP. 8 Support or lead improvement initiatives within the department, organization and/or pharma industry. 9 Prepare abstracts, posters, oral presentations and written reports to effectively communicate results of clinical programs and studies to internal and external stakeholders and colleagues with varying levels of clinical research knowledge. Education PhD or MS in Biostatistics, Statistics or related field Experience -PhD with 8 years of experience or MS with 11 years of experience in drug development -Experience providing statistical leadership at compound/indication level -Demonstrated statistical expertise and leadership in facilitating and optimizing the (pre/early/full-) clinical development strategy -Solid experience in applications of advanced statistical methodologies -Leading roles in regulatory submissions -Experience in interactions with major regulatory authorities preferred -Experience with CROs (either managing a CRO, or having worked in a CRO) or managing internal deliveries preferred -Track record of innovation preferred Competencies -Familiarity with regulatory guidance and interactions -Broad knowledge of clinical development and processes -Ability to collaboratively work and provide leadership in matrix environment -Strong interpersonal and communication skills (verbal and written in English) -Good working knowledge of SAS and/or R -Expertise in a range of statistical methodologies -Demonstrated use of innovative / creative methodology for analysis of clinical data -Familiarity with relevant regulatory guidance documents -Expertise in -CDISC, statistical programming, and/or data standards CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives. CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries. To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit ___ and CSL Plasma at ___. Our Benefits For more information on CSL benefits visit ___. You Belong at CSL At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. To learn more about inclusion and belonging visit Equal Opportunity Employer CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit ___.

Position Purpose: The Senior Programmer for Data Validation supports cross-functional teams such as Statistics, Data Management and Standards by overseeing and ensuring the quality of clinical data build and programming activities across in-house, hybrid, and vendor-supported studies. The role focuses on governance, review, and validation of deliverables to ensure alignment with CSL standards, regulatory requirements, and industry best practices. The incumbent applies strong expertise in CDASH and SDTM mapping, eCRF development, and EDC systems (e.g., Medidata Rave, Veeva Vault) to validate datasets, specifications, and vendor artifacts. The role will contribute to shaping future-state data capabilities by supporting initiatives around scalable data platforms and AI-driven automation, enabling more efficient and intelligent use of clinical data. Reporting Relationships: This role reports to: * Senior Director, Programming * Director, Programming - Center of Excellence Work Environment: *** On site / Hybrid at CSL Behring requires a minimum of 3 days in the designated work location office weekly for this role. Relocation and mobility assistance is not provided. Main Responsibilities and Accountabilities: * Collaborate with clinical study teams, Standards, and cross-functional stakeholders to define, implement, and continuously enhance data quality methods, acceptance criteria, and validation rules for eCRF and external data sources across all study models * Oversee the implementation and maintenance of data quality control frameworks, including validation check libraries and acceptance criteria for vendor and internally generated data, ensuring alignment with CSL standards and regulatory expectations * Govern and maintain a standardized library of reports and listings to support study teams, ensuring consistency, reusability, and efficiency across in-house, hybrid, and vendor-supported studies * Oversee the setup, automation, and monitoring of recurring data quality and operational reports across different models (in-house vs outsourced etc.)a ensuring accuracy, completeness, and timely availability of outputs * Partner with Data Management, Statistics, and vendors to review and validate clinical data deliverables, ensuring submission readiness in accordance with regulatory standards (e.g., SDTM, ADaM, define.xml) * Lead the development and oversight of data visualization and reporting solutions that provide insights into data quality, study progress, and key metrics to support informed decision-making * Ensure appropriate data structures, storage, and integration approaches that enable pooled analyses, traceability, and efficient retrieval of both current and legacy clinical data * Serve as a subject matter expert in CDASH, SDTM mapping, and EDC systems, providing guidance on data standards, eCRF design, and validation approaches to internal teams and external partners * Support the integration and governance of external data sources (e.g., IxRS, eDiaries, labs, ECG), ensuring data consistency, quality, and alignment with study requirements, while facilitating collaboration between internal teams and vendors * Contribute to innovation and future-state initiatives by supporting the development of scalable data platforms, automation strategies, and AI-enabled capabilities to enhance data processing, validation, and analytics Job Qualifications and Experience Requirements: Education * BSc in Computer Science, Mathematics, Statistics or related area with relevant experience * Other degrees and certifications considered if commensurate with related programming experience Experience * 5+ years of relevant experience (clinical data management, clinical programming, or a related function within a pharmaceutical or CRO environment, with exposure to in-house, hybrid, and/or vendor-supported study models) * Strong understanding of clinical data processes, including data standards, data flows, and integration of eCRF and external data sources, data quality oversight, validation processes, and vendor deliverable review * Proficiency in SAS and familiarity with Python, R, or C# is a plus to support automation and advanced analytics * Solid knowledge of CDISC standards, including CDASH, SDTM, and ADaM, with practical experience in data mapping, validation, and submission readiness * Familiarity with EDC systems (e.g., Medidata Rave, Veeva Vault) and understanding of eCRF design and clinical data collection frameworks * Demonstrated ability to manage priorities, meet timelines, and operate effectively in a fast-paced and evolving environment Competencies * Good communication and analytical skills * Good planning and organizational skills * Ability to work successfully in a matrix organizational structure * Networking skills and ability to share knowledge and experience amongst colleagues * Fluent in English, oral and in writing The expected base salary range for this position at hiring is $143,000 - $169,000. Please note this salary range reflects the minimum and maximum base pay that CSL expects to pay for this position at the listed for the Waltham, MA USA work location at the time of this posting. Individual base salary for a successful candidate is determined by qualifications, skill level, experience, competencies and other relevant factors. In addition to base salary, total compensation for this role may also include incentive compensation and equity. #LI-HYBRID CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives. CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries. To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit ___ and CSL Plasma at ___. Our Benefits For more information on CSL benefits visit ___. You Belong at CSL At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. To learn more about inclusion and belonging visit Equal Opportunity Employer CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit ___.

CSL's R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, we’re building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide. Could you be our next Specialist, R&D Contracts & Business Operations? The job is in our King of Prussia, PA, Maidenhead, UK or Melbourne AU office. This is a hybrid position and is onsite three days a week. You will report to the Associate Director R&D Contracts and Business Operations. Responsibilities: * Manage end-to-end business operations tasks for R&D contracts including required internal approvals, new vendor setup, contract execution, PO creation, and invoice resolution. * Draft and prepare a variety of contract templates (e.g., CDA, Service, Sponsorship, and HCP Agreements) in compliance with internal guidelines. * Collaborate with R&D stakeholders to ensure tracking and fulfillment of contractual obligations and responsibilities as outlined in executed agreements. * Serve as a liaison with Procurement and Compliance to ensure all necessary approvals are in place prior to contract execution. * Create, manage, and monitor POs for assigned functional areas, ensuring alignment with CSL processes and timely vendor payments. * Maintain contract records in the central portal and conduct periodic audits to ensure accuracy and completeness. * Support intake and data maintenance to enable reliable tracking and reporting of key operational metrics. * Foster effective communication with internal and external partners to ensure transparency, compliance, and timely decision-making. * Promote operational excellence by building collaborative relationships across global R&D and enabling functions. Qualifications:Requiared: * Bachelor’s degree in Business, Finance, Life Sciences, or related field. * 3+ years of experience in contract administration or business operations, preferably within the pharmaceutical or biotechnology industry. * Understanding of contract templates, key contract terms and conditions, and contract lifecycle management (CLM) tools. * Working knowledge of basic compliance principles and financial systems. * Proficiency with enterprise software platforms (e.g., Ariba, SAP, or equivalent). * Strong organizational skills, attention to detail, and ability to manage multiple priorities. #LI-HYBRID CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives. CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries. To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit ___ and CSL Plasma at ___. Our Benefits For more information on CSL benefits visit ___. You Belong at CSL At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. To learn more about inclusion and belonging visit Equal Opportunity Employer CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit ___.

The Senior Manager, Portfolio Insights & Analytics , will play a pivotal role in driving the strategic direction and performance of our portfolio management processes in support of R&D. Working closely with the Director, Portfolio Insights & Analytics and the Director, Portfolio Decision Strategy, this position is responsible for overseeing portfolio master data, ensuring adherence to standard portfolio processes, and delivering comprehensive performance reporting. In addition, this position provides hands-on decision analysis capabilities, with an explicit opportunity to build decision analysis skills over time. The ideal candidate will possess strong analytical skills, a keen eye for detail, and the ability to translate complex data into actionable insights. Primary Responsibilities and Accountabilities: Portfolio Master Data Management: • Oversee the maintenance and accuracy of portfolio master data, • Ensure data integrity and consistency with portfolio data classification and definitions., • Document, socialize and continuously improve standard portfolio management processes, • Identify opportunities to streamline workflows and enhance Portfolio Management systems, • Ensure compliance with established processes and guidelines., • Implement robust performance monitoring and evaluation mechanisms to analyze portfolio performance to identify risks, trends, opportunities, and trade-offs., • Define and measure key performance indicators (KPIs) aligned with strategic objectives to assess portfolio progression and value contribution, • Lead generation of standard PRISM Portfolio Executive Reporting materials on a monthly basis, • Become a Super User of Advanced Portfolio Analytics Tool (Planview Advisor), • Provide analytical and tactical support for Decision Analysis workshops, including preparation, in‑session support, and post‑workshop analysis and modeling Education and Experience: Bachelor’s degree in Business, Life Sciences, Data or related discipline (required); Advanced degree such as MBA or equivalent business qualification (preferred). Experience (7+ years) in R&D portfolio management, business analytics, data science, or related field Experience working in a global biotech organization / understanding of drug development lifecycle and commercialization process (required), global pharmaceutical market and competitive dynamics (strongly preferred) Demonstrated problem-solving skills including problem definition, hypothesis generation/ testing and solution proposition. Knowledge and experience in portfolio management software and affinity for leveraging new technology, automation, visualization tools and techniques (e.g. Power BI, Tableu, Qlik) Competencies: Effective collaboration and communication skills, with the ability to work productively within cross-functional teams and support collective goals. Proven experience in managing large datasets and ensuring data quality. Experience synthesizing quantitative and qualitative information into clear insights Curiosity and learning orientation, with interest in building decision analysis capabilities over time Strong analytical and problem-solving skills, including experience in forecasting, scenario planning, and modeling. Working Environment: Hybrid (minimum 3 days/week in office) Operate in a fast-paced, global, matrixed environment requiring coordination with stakeholders across time zones and geographies Manage relationships and interactions with senior leaders across R&D, Commercial Development, Finance, and Business Development Travel Expectations: Minimum travel for internal meetings, as required. CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives. CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries. To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit ___ and CSL Plasma at ___. Our Benefits For more information on CSL benefits visit ___. You Belong at CSL At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. To learn more about inclusion and belonging visit Equal Opportunity Employer CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit ___.

The Senior Statistical Programmer is responsible for providing hands-on support and technical guidance on clinical study teams. The development of study and ad hoc output including, but not limited to: ADaM datasets, tables, figures and listings output and/or QC of requested output is the main focus of this role. This individual, working closely with the study statistician will be responsible for review and acceptance of contract research organization (CRO) deliverables which are mainly, but not limited to, datasets in submission ready standard format (ADaM), tables, figures and listings and submission packages. This individual will participate in the design, development and quality control process for SAS programs used to access, extract, transform, review, analyze and submit clinical data for all requested analyses. This individual will interface with other departments (eg, Biostatistics, Data Management, Regulatory Operations, Medical Writing, ESP teams) to ensure Standard Operating Procedures are followed and the correct study data are used for all requests. This individual will participate in department and cross functional technology development and process improvement initiatives. Main Responsibilities and Accountabilities: • Collaborates with the study statistician to design data structure and specifications for ad hoc and study deliverables including, but not limited to ADaM datasets, Tables, Figures, Listings and Analysis Submission content. Leads the production and validation efforts for the designed output, this may include oversight of work by CROs., • Collaborates with peers and statisticians to ensure the quality and accuracy –thus submission readiness –of clinical data as required by authorities (i.e. SDTM, ADaM, tables, figures, listings, define.xml). Supports the review of related deliverables when provided by CROs., • Leads requested efforts for pooled and exploratory analyses working closely with clinical programming team and their collection of legacy data., • Leads the in-house specification and delivery of ISS and ISE datasets and associated output (tables, figures and listings) when not provided by CRO., • Leads the design and implementation of complex SAS programs for applications designed to analyze and report complex clinical trial data in CDISC ADaM format., • Identifies problems and develops global tools that increase the efficiency and capacity of the Statistical Programming group., • Works closely with clinical study teams to ensure that project timelines are met with high quality deliverables. Additional tasks Supports CR&D staff in data analysis requests. Performs additional statistical analyses including but not limited to: • Support responses to regulatory agencies, • Generate integrated summary of safety and efficacy, • Support publications and presentations, • Support planning and reporting of clinical trials via exploratory analyses of available data, • Replicate CRO and CSL statistician analyses for QC Job Qualifications and Experience Requirements: Education • BSc in Computer Science, Mathematics, Statistics or related area with relevant experience, • Other degrees and certifications considered if commensurate with related programming experience Experience • At least 5 years of experience in either clinical programming and/or statistical programming, within the CRO/pharmaceutical environment using SAS Software., • Understanding of clinical programming and/or statistical programming processes and standards., • Experiences with statistical programming using the SAS software including development and use of SAS Macros., • Knowledge in CDISC standards (CDASH, SDTM, ADaM)., • Ability to work effectively in a team setting, and to meet set goals by managing own timelines., • Ability to work in cross-functional, multicultural and international clinical trial teams. Competencies • Good communication and analytical skills., • Good planning and organizational skills., • Ability to work successfully in a matrix organizational structure., • Networking skills and ability to share knowledge and experience amongst colleagues., • Fluent in English, oral and in writing. Work Environment: On Site / Hybrid Required to be onsite in work location a minimum of 3 days a week. The expected base salary range for this position at hiring is $143,000 - $169,000. Please note this salary range reflects the minimum and maximum base pay that CSL expects to pay for this position at the listed Work Location for Waltham, MA at the time of this posting. Individual base salary for a successful candidate is determined by qualifications, skill level, experience, competencies and other relevant factors. In addition to base salary, total compensation for this role may also include incentive compensation and equity. #LI-HYBRID CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives. CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries. To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit ___ and CSL Plasma at ___. Our Benefits For more information on CSL benefits visit ___. You Belong at CSL At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. To learn more about inclusion and belonging visit Equal Opportunity Employer CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit ___.

The Associate Director (AD), Biostatistics, leads the full scope of statistical contribution to a clinical development program. The AD provides statistical strategies for the clinical trials and regulatory submissions, and is accountable for the statistical deliverables within the program. • Lead full scope of Biostatistics conduct for the responsible program within a therapeutic area., • Define statistical strategy and ensure appropriate statistical methodologies applied to study design and data analysis for clinical trials and regulatory submissions, • Influence and contribute to clinical development plans, collaborate with cross-functional team for governance reviews., • Lead statistical strategy for planning and study execution (member of Study Executive Team, Clinical Development Team) and quantitative evaluation to clinical trials, regulatory submissions, and related documents., • Provide statistical thought partnership for innovative study design and clinical development plans, including Go-No Go criteria and probability of technical success calculations., • Provide for project-wide planning of analyses; quality and timely delivery of interim and final results, including integrated analyses for submissions., • Represent Biostatistics in interactions with regulatory authorities (eg, FDA, EMA, PMDA), • Be responsible for interpreting analysis results and ensuring reporting accuracy in study reports and regulatory documents., • Manage outsourcing operations or work with internal statistical programmers within the responsible program. Ensure timeliness and quality of deliverables by CRO/FSP., • Support or lead improvement initiatives within the department, organization and/or pharma industry., • Prepare abstracts, posters, oral presentations and written reports to effectively communicate results of clinical programs and studies to internal and external stakeholders and colleagues with varying levels of clinical research knowledge. Experience and Qualifications Education PhD or MS in Biostatistics, Statistics or related field Experience -PhD with 8 years of experience or MS with 11 years of experience in drug development -Experience providing statistical leadership at compound/indication level -Demonstrated statistical expertise and leadership in facilitating and optimizing the (pre/early/full-) clinical development strategy -Solid experience in applications of advanced statistical methodologies -Leading roles in regulatory submissions -Experience in interactions with major regulatory authorities preferred -Experience with CROs (either managing a CRO, or having worked in a CRO) or managing internal deliveries preferred -Track record of innovation preferred Competencies -Familiarity with regulatory guidance and interactions -Broad knowledge of clinical development and processes -Ability to collaboratively work and provide leadership in matrix environment -Strong interpersonal and communication skills (verbal and written in English) -Good working knowledge of SAS and/or R -Expertise in a range of statistical methodologies -Demonstrated use of innovative / creative methodology for analysis of clinical data -Familiarity with relevant regulatory guidance documents -Expertise in -CDISC, statistical programming, and/or data standards CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives. CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries. To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit ___ and CSL Plasma at ___. Our Benefits For more information on CSL benefits visit ___. You Belong at CSL At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. To learn more about inclusion and belonging visit Equal Opportunity Employer CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit ___.

This position will lead the transformation of project leadership capabilities across the R&D enterprise. On a systemic level, this role will prepare critical GPL roles (Exec Directors) to be CEO of the project via a bespoke leadership/drug development/executive training and coaching program which will equip these leaders and associated project teams to navigate ambiguity, prioritize effectively, and make high-impact R&D investment decisions that accelerate innovation and deliver value to patients. This position will work with the CEO/GLG, RDLT and all levels to ensure the Project Operating Model is continuously improved for simple, rapid, empowered, project-centric decision making at the right level. This role will also lead the leadership development of Project Managers (PMs) and Research Project Leads (RPLs) in R&D and strengthen the GPL/GPM partnership. Main Responsibilities & Accountabilities -Develop and run an executive leadership/coaching/"continuous improvement" program to actualize GPL role as "CEO" of the program•Work with senior leaders, TA Co-Leads and partners and beyond R&D to ensure the behaviors and decision making of R&D aligns to the Project Operating Model•Continuously improve the project operating model at all levels to ensure rapid, effective project centric decisions•Support the entire R&D project community (inside and outside R&D) with appropriate change management driving a project-focused culture, incentives/rewards practices, and communications•Accountable for development and stewardship of the Project Operating Model, including education, guidance, implementation and modification (when needed) while also ensuring optimal application of the project axis and team structure•Develop frameworks for R&D Project Management excellence. Primary focus is R&D Project Management within POE while serving as extended Centre of Excellence on Project Management best practices across R&D •Oversee the Operation of the PM Academy, curriculum, system, needs analysis etc. to support elevating the craft of Project Management in R&D. Recommends capability areas for focused training, certification options/requirements and consistency of practice across the organization•Build frameworks and culture to strengthen the GPL/GPM partnership•Build a culture and frameworks to elevate the role of PMs & RPLs within R&D•Serves as point of contact for TA Co-Leads for the establishment or dissolution of Product/Platform Strategy Teams and decision making by the Head of R&D•Enabling a culture of high-performing teams. Lead culture change, promoting shared values and collaboration, supporting the shift from functional-focus to project-focus•Partner with R&D leaders and TA Co-Leads to optimize the interface between the project and the functional axes•Define a strategy for building main skills across Project Excellence; identify targeted R&D project-focused audiences and associated learning goals; develop a planned schedule of offerings to meet our needs•Develop and run a training and "continuous improvement" program for all PST members to drive standardization of best practices Qualifications & Experience Requirements -Bachelor’s or Master’s in science, operations, or business-related field•12+ years in R&D operations, vendor management or business support•Experience with research vendors and lab operations•Strong coordination skills with enabling functions•Experience working in cross-functional R&D teams CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives. CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries. To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit ___ and CSL Plasma at ___. Our Benefits For more information on CSL benefits visit ___. You Belong at CSL At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. To learn more about inclusion and belonging visit Equal Opportunity Employer CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit ___.

CSL's R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, we’re building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide. Could you be our next Associate Director, Programming (Macros & Automation)? The job is in our Waltham MA, King of Prussia PA or Glattbrugg Switzerland Office. This is a hybrid position and is onsite a minimum of three days a week. You will report to the Director, Programming. Position Purpose: You will be responsible for designing new programming standards, implementing them across the programming organization, and taking full ownership of existing shared codebases and automation frameworks that support clinical data processing, metadata management, reporting, and visualization workflows. You will be a hands-on technical leader who can architect scalable reusable macro frameworks, modernize legacy code, and ensure consistent, efficient, and compliant programming practices aligned with CDISC and regulatory expectations across the programming organization. In addition, a deep expertise in SAS macro development to lead and govern enterprise programming standards and automation solutions. Main Responsibilities and Accountabilities: 1. Programming Standards Leadership * Define, implement, and maintain enterprise programming and analysis standards. * Develop scalable, reusable macro-driven frameworks to standardize programming activities across studies and programs. Represent programming at the standards governance forums and drive organization-wide adoption of programming standards and best practices 2. Automation & Code Ownership * Take ownership of existing SAS macro libraries, tools, and automation solutions. * Maintain, enhance, and modernize legacy programming frameworks to improve reliability, maintainability, and efficiency. Establish documentation, validation, version control, and support processes for all programming automation assets. 3. Operational Support * Provide programming oversight for daily Statistical Computing Environment (SCE) activities in partnership with technology and support teams. * Ensure the environment effectively supports standards execution and automated workflows. 4. Cross-Functional Collaboration & Compliance * Collaborate with data management, statistics, clinical, and quality teams to ensure programming practices align with CDISC standards, organizational procedures, and regulatory expectations. * Serve as the subject matter expert for programming standards during internal reviews, audits, and inspections. * Track and report adoption and effectiveness of standards using defined metrics. 5. Continuous Improvement * Drive simplification and consistency of programming processes through automation and reusable solutions. * Develop training materials, guidance, and best practices to support consistent implementation. * Identify opportunities to improve reporting and visualization approaches through standardized methods. Job Qualifications and Experience Requirements: Education : * BSc in Computer Science, Mathematics, Statistics or related area with relevant experience * Other degrees and certifications considered if commensurate with related programming experience Experience: * 9+ years of experience in either clinical programming and/or statistical programming, within the CRO/pharmaceutical environment using SAS Software. * Comprehensive understanding of clinical programming and/or statistical programming processes and standards. * Expert-level SAS programming with advanced macro development capability (required). * Demonstrated experience designing reusable programming frameworks and shared automation utilities. * Experience managing large shared code repositories and supporting enterprise programming tools. * Fluency in technical requirements for CDISC Compatible Data Sets and DDT Files * Strong understanding of CDISC principles and working within regulated clinical development environments. * Familiarity with additional scripting or analytical tools (e.g., R or Python) is beneficial. * Experience Supporting programming standard governance and systems operations * Experience working in a global organization preferred Competencies • Broad knowledge of clinical development and processes, • Strong interpersonal and communication skills (verbal/written/presentation in English); including cross functional and senior management., • Presentations of programming techniques at professional conferences is a plus, • Ability to work collaboratively in matrix environment, • Solutions oriented mindset The expected base salary range for this position at hiring is $189,000 - $220,000. Please note this salary range reflects the minimum and maximum base pay that CSL expects to pay for this position at the listed for Waltham MA at the time of this posting. Individual base salary for a successful candidate is determined by qualifications, skill level, experience, competencies and other relevant factors. In addition to base salary, total compensation for this role may also include incentive compensation and equity. #LI-HYBRID CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives. CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries. To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit ___ and CSL Plasma at ___. Our Benefits For more information on CSL benefits visit ___. You Belong at CSL At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. To learn more about inclusion and belonging visit Equal Opportunity Employer CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit ___.

of2 CSL's R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, we’re building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide. As the Senior Manager, R&D Outsourcing is responsible for managing the full contracting lifecycle for strategic outsourced R&D services and projects across assigned therapeutic and functional areas. This includes drafting, reviewing, and negotiating scopes of work, budgets, and contracts with external service providers to support CSL’s global clinical and portfolio development needs. This individual contributor role partners closely with Business Strategy Leads, Project Owners, Legal, Finance, and Procurement to ensure timely contract execution, cost control, and compliance with CSL’s policies and standards. Key Responsibilities Outsourcing Execution Manage vendor identification, RFI/RFP processes, proposal reviews, and budget and contract negotiations for strategic outsourced R&D services (e.g., MSAs, Work Orders, Change Orders, rate cards). Draft, review, and finalize contracts to ensure timely execution and compliance with CSL policies. Coordinate with project teams and stakeholders to align contract deliverables with operational needs. Contract Oversight and Compliance Track contractual obligations and ensure vendors meet agreed terms, budgets, and timelines. Support resolution of contract or performance issues in collaboration with Legal, Finance, and project stakeholders. Maintain organized and up-to-date contract documentation in line with internal requirements and industry regulations. Financial and Operational Support Review vendor proposals and budgets for accuracy and alignment with scope. Monitor ongoing vendor spending versus approved budgets; highlight variances as needed. Support financial forecasting and reporting by providing timely contract and spend data. Cross-Functional Collaboration Partner with Business Strategy Leads, Project Owners, Legal, Finance, and Procurement to ensure smooth contract operations. Communicate contract requirements and processes clearly to internal stakeholders. Serve as a resource for questions on contract terms, templates, and procedures. Process Improvement and Reporting Identify opportunities to improve contracting efficiency, consistency, and compliance. Contribute to tracking and reporting of outsourcing metrics and performance indicators. Participate in cross-functional initiatives to enhance vendor management practices. Skills and Experience Required Minimum 7 years of experience managing end-to-end contracting with R&D service providers (e.g., CROs). Proven ability to draft, review, and negotiate budgets and contracts. Working knowledge of clinical trial operations and vendor cost structures. Strong attention to detail, organizational skills, and ability to manage multiple priorities. Excellent communication and collaboration skills across functional teams. Preferred: Experience supporting outsourcing in global or matrixed R&D organizations. Familiarity with contract lifecycle management software or financial systems. Understanding of basic financial principles (e.g., budget tracking, forecasting). Qualifications and Education Required Bachelor’s degree in Business, Finance, Life Sciences, or a related field CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives. CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries. To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit ___ and CSL Plasma at ___. Our Benefits For more information on CSL benefits visit ___. You Belong at CSL At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. To learn more about inclusion and belonging visit Equal Opportunity Employer CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit ___.

Main Responsibilities & Accountabilities: Responsible for leading the successful operational delivery of global, cross-functional R&D projects of strategic importance to CSL’s product portfolio. Main Responsibilities & Accountabilities Work closely with project leader to define strategy and operational tactics Responsible for the preparation and management of project budgets, sensitivities, resources, project timelines, project scope and all other project documentation Accountable for the accuracy and quality of reports to senior stakeholders Lead cross functional development teams through tactical execution of project plans Identify, manage and resolve project issues and mitigate risks Ensure documentation of key team information, decisions, actions, modifications to scope, resources, timelines and milestones in project management systems is current. Identify, evaluate the critical path, scenarios and challenge assumptions to increase robustness of project plans Monitor performance vs. plan (budget and timeline) Coordinate program updates to Sr. Management Provide coaching and mentorship to more junior members of the R&D Global Project Management Department Qualifications & Experience Requirements Required: Bachelor degree or equivalent in Science, Engineering, or a related field. Preferred: An advanced degree (MSc, PhD) in Science or related field, Masters of Business Administration (MBA) or equivalent Project Management Professional (PMP) certification, 7+ years’ experience in the biotechnology or pharmaceutical industry 5+ years’ experience as a project manager leading cross-functional project teams in a matrixed, global environment, In-depth knowledge in drug research, development and manufacturing processes Demonstrated experience in delivering projects to meet business objectives on time, within budget and with quality. Outstanding influencing ability & collaboration skills Proven success with building and developing matrix teams. Ability to work effectively in a matrix environment that includes interactions with multiple stakeholder groups Excellent executive presence, communication & change management skills. Exemplary project management skills Highly proficient in the use of Project Management processes and tools (e.g. Microsoft Project). CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives. CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries. To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit ___ and CSL Plasma at ___. Our Benefits For more information on CSL benefits visit ___. You Belong at CSL At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. To learn more about inclusion and belonging visit Equal Opportunity Employer CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit ___.

CSL's R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, we’re building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide. You will oversees all areas of single case processing in the global pharmacovigilance database from all sources. This includes ensuring that the vendor performs case processing in accordance with regulatory guidelines, PV agreements, and the Company's SOPs, as well as responding to specific questions or queries about cases. This role develops standards and processes, with a focus on global compliance and process optimization. Oversees Medical Evaluators responsible for medical review of ICSRs. Key Responsibilities Oversight of Case Management Processes activities Oversight of Medical Evaluator role which completes medical review of the following ICSRs: All serious cases from all sources Non-serious cases from company-sponsored clinical study, if required Legal ICSRs (serious and non-serious) Reportable cases of combination products with device issue(s) / malfunction (serious and non-serious) Non-serious ICSRs are processed by Case Managers and reviewed for correct seriousness on an aggregate basis by Medical Evaluator Medical review includes: Review of seriousness, listedness and causality assessments Review of event terms and MedDRA coding Review of narrative for medical accuracy and consistency Assessment of the need for Quality Investigations Generation of medical follow up queries / Targeted Questionnaires Drive department-wide planning: resource, budget, and org. strategy Own case management dashboards and governance scorecards Prepare for internal and external inspections including coordination of creation of presentations Lead transformation initiatives (e.g., vendor transitions, digital tools) Monitor regulatory trends and represent PV case management in global initiatives Coordinate departmental leadership meetings and communication Pilot innovations (e.g., RPA, AI triage, tech integration) Align with Clinical, QA, Regulatory, and Safety Science functions Coordinate creation and update of SOPs Retain product and process knowledge Skills and Education Required Minimum of 10 years of Clinical Trial and Post-marketing Pharmacovigilance (PV) experience with 5 years of managerial/leadership experience Global pharmacovigilance database knowledge is required along with proficient knowledge of global and local regulatory rules and regulations Qualifications and Education Required BS/BA, RN, Pharmacist, or similar CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives. CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries. To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit ___ and CSL Plasma at ___. Our Benefits For more information on CSL benefits visit ___. You Belong at CSL At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. To learn more about inclusion and belonging visit Equal Opportunity Employer CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit ___.

CSL's R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, we’re building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide. The Director Clinical Operations Lead is accountable for the development of the operational strategy for a clinical study(ies) and/or a clinical program (s) as well as the end-to-end study management and delivery of all operational activities and budget management relating to assigned clinical study (ies)/program(s). Responsibilities encompass support to the development of the operational strategy for our most complex studies and ensuring achievement of all program goals within established timelines, budget, and quality standards, and according to the TA strategies. This role must be experienced in working in a matrix environment (internal and external partners) with cross-functional responsibilities associated with trial execution and overall therapeutic area clinical development planning. Strong communication and presentation skills are required. Main Responsibilities and Accountabilities: * Clinical Operations Strategy: Design and implement operational strategies, study management plans, and supporting documentation to drive study efficiency and quality (most complex studies). Continuously assess and improve clinical operations processes. Provide early input in CDP and study outline. * Project Management & CRO oversight: Lead cross-functional study teams, coordinate with functional area representatives, and ensure timely execution of all study-related activities. Responsible for vendor selection/management/oversight, issue escalation, and inspection readiness. * Stakeholder Management & Team Leadership: Lead and coordinate cross-functional teams, fostering collaboration among internal and external stakeholders (including vendors, investigators, and regulatory authorities). Act as the primary point of contact for all study-related matters, build and maintain strong relationships, mentor and support team members, and represent the study team in communications with senior management. Act in an advisory capacity to other clinops colleagues and ensure knowledge sharing across therapeutic areas. Be the clinops voice at PST/TALT. * Budget Forecasting and Performance Management: Forecast, manage, and report on study budgets and key performance metrics, including study start-up, enrollment, and data collection timeliness/quality. Engage with key project stakeholders, including GPLS, TALT leads, Finance, POE. Drive accuracy and reliability in terms of budget. * End-to-End Clinical Study Management: Plan, manage, and execute our most complex global clinical studies from protocol development through to Clinical Study Report (CSR) completion and Trial Master File (TMF) archiving. Oversee timelines, budgets, regulatory/GCP compliance, feasibility, country strategy, enrollment plans, and risk mitigation. * Act as the primary point of contact both internally and externally (e.g. vendors) as applicable for anything study/program/asset related. * Provide regular study status updates including critical issues to senior leadership as needed while providing support to the study team with stakeholder management and issue escalation. Portray strong and confident communication and presentation skills. Audiences will include those both internal and external partners. * Support audits/inspections and resolutions of findings. * Contribute to the leadership of the Clinops function in key areas of change and continuous improvement. May be asked to lead cross functional change initiatives. Support in the development of new SOPs, guidelines etc and/ or participate in working groups about new processes and change initiatives. * Functional leadership and mentorship of junior staff required; Act in advisory capacity to other clinops colleagues within and across TAs. * Acts as an integral resource for clinops members and ensures that cross-functional process efficiencies are identified and maximized in accordance with project goals and that compliance is maintained. Job Qualifications and Experience Requirements Education At minimum, bachelor’s degree or equivalent in life science, nursing, pharmacy, medical laboratory technology, or other health/medical related area preferred. Other degrees and certifications considered if commensurate with related clinical research experience (e.g., diploma or associate degree RN, certified medical technologist). Experience * Demstrable xperience in overseeing large and/or complex global clinical trials. * As a guide, a minimum of 14 years’ relevant clinical research (or related) experience within the pharmaceutical industry. * Previous experience in leading and managing a team of professional staff. * A solid understanding of the drug development process, and specifically, each step within the clinical trial process. * Robust budget forecasting and management experience. * Thorough knowledge of ICH guidelines/GCP and its applicability to all stages of the clinical development process Competencies * Demonstrated ability to lead teams and work in a fast-paced team environment. * Experienced in working within a Matrix Environment and ability to work through interpersonal difficulties and resolve conflicts with a Matrix Environment * Successfully demonstrated the ability to mentor and coach others through peer-to-peer interactions and to develop reporting personnel to grow in complex clinical project management capabilities. * Ability to evaluate, judge and make decisions regarding staff. Ability to teach/coaching and setting an example of ‘best practice’. * Excellent interpersonal and decision-making skills. * Demonstrates innovation. Possesses drive, energy, and enthusiasm to deliver the program objectives. * Skilled at independently navigating new or novel indications, study/program approaches, and unique challenges. * Excellent understanding of all tasks involved in a clinical development program(s) from developing a protocol through to finalizing a clinical study report. * Ability to plan and ensure execution and completion of clinical program(s) to the highest ethical and scientific standards. * Demonstrated ability to comprehend complex scientific concepts and data. Proficient in reviewing and assessing clinical data. * Extensive and comprehensive knowledge of ICH guidelines/ GCP, Maintains current medical/scientific/regulatory knowledge. * Demonstrated project management skills including simultaneous management of multiple projects. Possesses excellent planning, time management & coordination skills. * Demonstrated ability to problem solve and use clear judgment in relation to interactions with external parties, timelines, and complex clinical programs. * Excellent written and oral communication skills and maintains computer literacy in appropriate software. CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives. CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries. To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit ___ and CSL Plasma at ___. Our Benefits For more information on CSL benefits visit ___. You Belong at CSL At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. To learn more about inclusion and belonging visit Equal Opportunity Employer CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit ___.

The Associate Director (AD), Biostatistics, leads the full scope of statistical contribution to a clinical development program. The AD provides statistical strategies for the clinical trials and regulatory submissions and is accountable for the statistical deliverables within the program. ( Positions available supporting multiple Therapeutic Areas available ) Main Responsibilities: • Lead full scope of Biostatistics conduct for the responsible program within a therapeutic area. Define statistical strategy and ensure appropriate statistical methodologies applied to study design and data analysis for clinical trials and regulatory submissions, • Influence and contribute to clinical development plans, collaborate with cross-functional team for governance reviews., • Lead statistical strategy for planning and study execution (member of Study Executive Team, Clinical Development Team) and quantitative evaluation to clinical trials, regulatory submissions, and related documents., • Provide statistical thought partnership for innovative study design and clinical development plans, including Go-No Go criteria and probability of technical success calculations., • Provide for project-wide planning of analyses; quality and timely delivery of interim and final results, including integrated analyses for submissions., • Represent Biostatistics in interactions with regulatory authorities (eg, FDA, EMA, PMDA), • Be responsible for interpreting analysis results and ensuring reporting accuracy in study reports and regulatory documents., • Manage outsourcing operations or work with internal statistical programmers within the responsible program. Ensure timeliness and quality of deliverables by CRO/FSP., • Support or lead improvement initiatives within the department, organization and/or pharma industry., • Prepare abstracts, posters, oral presentations and written reports to effectively communicate results of clinical programs and studies to internal and external stakeholders and colleagues with varying levels of clinical research knowledge. Education and Experience: • PhD with 8 years of experience or MS with 11 years of experience in drug development, • Experience providing statistical leadership at compound/indication level, • Demonstrated statistical expertise and leadership in facilitating and optimizing the (pre/early/full-) clinical development strategy, • Solid experience in applications of advanced statistical methodologies, • Leading roles in regulatory submissions, • Experience in interactions with major regulatory authorities preferred, • Experience with CROs (either managing a CRO, or having worked in a CRO) or managing internal deliveries preferred, • Track record of innovation preferred Competencies: • Familiarity with regulatory guidance and interactions -Broad knowledge of clinical development and processes, • Ability to collaboratively work and provide leadership in matrix environment -Strong interpersonal and communication skills (verbal and written in English), • Good working knowledge of SAS and/or R, • Expertise in a range of statistical methodologies, • Demonstrated use of innovative / creative methodology for analysis of clinical data, • CDISC, statistical programming, and/or data standards, • Biostatistics and Statistical Programming Operations CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives. CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries. To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit ___ and CSL Plasma at ___. Our Benefits For more information on CSL benefits visit ___. You Belong at CSL At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. To learn more about inclusion and belonging visit Equal Opportunity Employer CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit ___.

CSL's R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, we’re building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide. Could you be our next Associate Director, Regional Regulatory Lead-US? The job is in our King of Prussia, PA or Waltham MA office. This is a hybrid position and is onsite three days a week. You will report to the Director Global Regulatory Lead. You are a member of the respective GRA GRS Therapeutic Area and contributes to the vision and goals of CSL as: Regulatory leaders who leverage regional regulatory experience / expertise to influence and actively contribute to an innovative, scientifically sound, global, integrated regulatory vision / strategies for assigned product/s with a patient centric-focus, leveraging regional commercial insights and applying prudent risk-taking to ensure timely delivery of successful regulatory outcomes. Effectively partner with assigned product/s Global Regulatory Affairs Strategy Team (GRAST) GRL plus other regional, labeling and CMC GRAST members to ensure ‘One GRA Voice’, effective inputs into risk assessment and decision making. Ensures bi-directional communication with stationed region commercial operations and GRA. Directly engaging with health authority (HA) in stationed country (FDA or EMA), maintaining productive relationship with HA contacts and driving positive regulatory outcomes with respective HA for assigned product/s in conjunction with GRL. May lead product health authority interaction with support GRL or Regulatory TA Head. Partner with GRAST members to achieve regulatory deliverables (including leading assigned tasks) while fostering individual accountability, ‘team spirit’, actively contribute and executing on decisions expeditiously resulting in positive regulatory outcomes Responsibilities: * * * * Qualifications: A bachelor’s degree (four-year university degree) in pharmacy, biology, chemistry, pharmacology, clinical medicine or related life science is required. An advanced degree in a related field (MS, PhD or MD, DVM) or MBA is preferred. 10+ years’ experience in the biotech or pharmaceutical industry, with at least 5 years of regulatory experience, including 3 years working on developmental products. Experience in leading teams (preferred 3 years) as a direct or matrix manager, setting direction, holding people accountable and fostering a collaborative, empowered, team environment. Assess and recommend preferred option for tough decisions. Candidates have knowledge and understanding of pharmaceutical/biological product development and regulatory requirements for product development and approval in more than one key region (EU, US, Japan) Experience working in Regulatory Affairs with direct agency interaction responsibility with at least 1 health authority. The expected base salary range for this position at hiring is $185,000 - $210,000. Please note this salary range reflects the minimum and maximum base pay that CSL expects to pay for this position at the listed for Waltham MA at the time of this posting. Individual base salary for a successful candidate is determined by qualifications, skill level, experience, competencies and other relevant factors. In addition to base salary, total compensation for this role may also include incentive compensation and equity. #LI-HYBRID CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives. CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries. To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit ___ and CSL Plasma at ___. Our Benefits For more information on CSL benefits visit ___. You Belong at CSL At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. To learn more about inclusion and belonging visit Equal Opportunity Employer CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit ___.

Principal Programmer - Clinical Data Oversight & Standards provides leadership and oversight for clinical data build, programming, and vendor deliverables across in-house, hybrid, and outsourced studies, ensuring alignment with CSL standards, regulatory requirements, and industry best practices. The role drives governance, review, and validation processes; leads the implementation of CDASH and SDTM standards; and oversees scalable validation frameworks and data quality controls. Additionally, it ensures effective integration of internal and external data into platforms such as the CSL Clinical Data Warehouse, while advancing automation, AI-driven solutions, and strong cross-functional collaboration with Biostatistics, Data Management, Standards, and external partners Main Responsibilities and Accountabilities: • Leads and develops a team of Clinical Data Validation Programmers, providing direction on clinical data standards, validation, and oversight activities across in-house, hybrid, and vendor-supported studies., • Establishes and drives clinical data governance frameworks, including review and validation processes for eCRF builds, SDTM datasets, specifications, and vendor deliverables, ensuring compliance with internal standards, regulatory requirements, and industry best practices., • Oversees the development, implementation, and continuous improvement of clinical data standards (e.g., CDASH, SDTM) and associated validation check libraries to enable consistent, scalable, and high-quality data across studies., • Provides strategic oversight of data integration processes, including external data flows and system interfaces, ensuring accurate, efficient, and compliant data ingestion into downstream platforms such as the Clinical Data Warehouse., • Ensures submission readiness of clinical data by establishing robust quality control frameworks and validation processes aligned with regulatory expectations (e.g., SDTM, ADaM, define.xml)., • Develops, maintains, and governs departmental and cross-functional SOPs, standards, and QMS documentation related to clinical data oversight, standards, and programming., • Drives cross-functional alignment by partnering with Biostatistics, Data Management, Standards, and external partners to ensure consistent understanding and application of clinical data standards and quality expectations; provides guidance, knowledge sharing, and targeted training to support effective implementation across studies., • Provides oversight and guidance on data storage, archival, and retrieval strategies to support regulatory submissions, pooled analyses, and reuse of legacy data in collaboration with Biostatistics and other stakeholders., • Oversees programming and validation support to ensure availability of high-quality, analysis-ready datasets, while promoting automation, efficiency, and innovation through the use of SAS and emerging technologies (e.g., Python, AI-driven solutions). Job Qualifications and Experience Requirements: Education • Degree (BSc/MSc/Diploma) in Computer Science, Mathematics/Statistics, or related area with relevant experience., • At least 7 years of relevant experience (either clinical programming and/or statistical programming, within the CRO/pharmaceutical environment)., • Significant experience with demonstrated leadership or oversight responsibilities and a strong understanding of the end-to-end clinical data lifecycle, including data collection, validation, standards implementation, and regulatory submission requirements., • Proven expertise in CDISC standards (CDASH, SDTM, ADaM) and their practical application across studies, including review and oversight of datasets, specifications, and mappings., • Experience with EDC and/or Clinical Data Warehouse platforms (e.g., Medidata Rave, Veeva Vault), with a solid understanding of data flows, integrations, and database structures., • Proficiency in SAS programming, with working knowledge of Python, R, or similar languages preferred to support automation and advanced data review., • Demonstrated experience in establishing or applying data quality frameworks, validation processes, and governance models in a clinical data environment., • Proven ability to manage priorities, timelines, and team deliverables in a fast-paced environment, while driving continuous improvement and operational excellence., • Excellent communication and analytical skills., • Strong interpersonal and effective leadership skills., • Excellent organizational skills and ability to prioritize individual and team workloads., • Strong ability to lead and collaborate across cross-functional, global teams, including oversight of vendor deliverables and alignment with internal stakeholders such as Biostatistics, Data Management, and Standards., • Is able to identify and engage internal and external expertise as needed., • Proven networking skills and ability to share knowledge and experience amongst colleagues., • Strong written and verbal English communication skills Work Environment: On-Site Hybrid Requires a minimum of 3 days a week in office work location The expected base salary range for this position at hiring is $170,000 - $201,000 USD. Please note this salary range reflects the minimum and maximum base pay that CSL expects to pay for this position at the listed for Waltham, MA USA at the time of this posting. Individual base salary for a successful candidate is determined by qualifications, skill level, experience, competencies and other relevant factors. In addition to base salary, total compensation for this role may also include incentive compensation and equity. #LI-HYBRID CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives. CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries. To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit ___ and CSL Plasma at ___. Our Benefits For more information on CSL benefits visit ___. You Belong at CSL At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. To learn more about inclusion and belonging visit Equal Opportunity Employer CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit ___.

The Director, Biostatistics, leads the full scope of statistical contribution to a clinical development program, including life cycle management. The AD provides for statistical excellence in clinical development plans, trial planning, data analysis, interpretation and reporting, and regulatory interactions and submissions, while partnering closely with Clinical Development and other key stakeholders. Responsibilities and Accountabilities: -Define the statistical strategy and ensure appropriate statistical methodologies applied to the clinical development plan, study design and data analysis for clinical trials, and regulatory submissions. •Provide statistical insight into execution of clinical development, to ensure study conduct leads to a statistically sound and robust data package, maximize probability of program success. •Interprets analysis results and ensures reporting accuracy in study reports and regulatory documents, abstracts, posters, oral presentations, manuscripts and written reports to effectively communicate results of clinical programs and studies.•May serve as the point of contact for one or more PSTs within the TA.•Lead or provide oversight to the analysis delivery and quantitative evaluation of clinical trials, and integrated analysis. •Represent Biostatistics in interactions with regulatory authorities (eg, FDA, EMA, PMDA), which includes leading written responses to regulatory questions and attending regulatory meetings. Qualifications: Education PhD or MS/MA in statistics or related field Experience 10+ years of experience in clinical development within the pharmaceutical or biotechnology industry Demonstrated leadership in statistical contributions to clinical programs and regulatory submissions Experience partnering with cross-functional teams and interacting with health authorities Experience managing external partners (CROs, consultants) Competencies Strong statistical methodology knowledge and clinical trial design expertise Ability to collaborate and influence across functions and levels Excellent communication and interpersonal skills Experience with CDISC standards, programming oversight, and statistical operations Strategic and analytical mindset with a focus on execution Ability to work in a matrixed environment and lead through influence Working Conditions • Occasional travel to scientific conventions CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives. CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries. To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit ___ and CSL Plasma at ___. Our Benefits For more information on CSL benefits visit ___. You Belong at CSL At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. To learn more about inclusion and belonging visit Equal Opportunity Employer CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit ___.

CSL is transforming its R&D organization to accelerate innovation and create greater impact for patients. With a streamlined, project-led structure and a focus on collaboration, we're building a future-ready team that excels in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide. Could you be our next Associate Director, Project Management? The job is in our King of Prussia, PA or Maidenhead UK office. This is a hybrid position and is onsite three days a week. You will report to TA Portfolio Delivery Lead. Position Description: Responsible for leading the successful operational delivery of global, cross functional R&D projects of strategic importance to CSL's product portfolio. Main Responsibilities & Accountabilities: * * * * * * * * * * Qualifications and Experience * * * * #LI-HYBRID CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives. CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries. To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit ___ and CSL Plasma at ___. Our Benefits For more information on CSL benefits visit ___. You Belong at CSL At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. To learn more about inclusion and belonging visit Equal Opportunity Employer CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit ___.

The Principal Statistical Programmer is responsible for providing leadership and hands-on support in the development and maintenance of the CSL statistical programming capabilities which is required to meet regulatory obligations. The individual will work closely with the Associate Director, Director, and Statistical Programmers to build internal programming tools. This individual, working closely with the study team, will be responsible for review and acceptance of contract research organization (CRO) deliverables which are mainly, but not limited to, datasets in submission ready standard format (ADaM), tables, figures, listings and submission packages. This individual will provide expertise in the design, development and quality control process for SAS programs used to access, extract, transform, review, analyze and submit clinical data for all requested analyses. This individual will collaborate with other departments (eg, Biostatistics, Data Management, Regulatory Operations, Medical Writing, ESP teams) to ensure Standard Operating Procedures are followed and the correct study data are used for all requests. This individual will participate in department and cross functional technology development and process improvement initiatives. Main Responsibilities and Accountabilities: • Collaborates with the study teams to design data structure and specifications for ad hoc and study deliverables including, but not limited to ADaM datasets, Tables, Figures, Listings and Analysis Submission content. Plans and leads the production and validation efforts for the designed output, this may include oversight of work by CROs., • Collaborates with study teams to ensure the quality and accuracy – thus submission readiness – of clinical data as required by authorities (i.e. SDTM, ADaM, tables, figures, listings, define.xml). Supports the review of related deliverables when provided by CROs., • Leads and oversees requested efforts for pooled and exploratory analyses working closely with Statistics TA lead and/or study statisticians as well as with clinical programming team and their collection of legacy data., • Leads and oversees the in-house specification and delivery of ISS and ISE datasets and associated output (tables, figures and listings) when not provided by CRO., • Leads and oversees the design and implementation of complex SAS programs for applications designed to analyze and report complex clinical trial data in CDISC ADaM format., • Leads and oversees the development of global tools that will increase the efficiency and capacity of the Statistical Programming group. Collaborates with CR&D staff regarding data analysis requests. Performs additional statistical analyses including but not limited to: • support responses to regulatory agencies,, • generate integrated summary of safety and efficacy,, • support publications and presentations,, • support planning and reporting of clinical trials via exploratory analyses of available data,, • replicate CRO and CSL statistician analyses for QC Job Qualifications and Experience Requirements: Education • BSc in Computer Science, Mathematics, Statistics or related area with relevant experience, • Other degrees and certifications considered if commensurate with related programming experience Experience • At least 7 years of experience in either clinical programming and/or statistical programming, within the CRO/pharmaceutical environment using SAS Software., • In-depth understanding of clinical programming and/or statistical programming processes and standards., • In-depth understanding of regulatory requirements relevant to statistical programming (e.g. GCP, ICH)., • Extensive experience with statistical programming using the SAS software including development and use of SAS Macros. Strong programming and problem-solving skills., • Advanced knowledge in CDISC standards (CDASH, SDTM, ADaM)., • Proven experience in leading programming activities for pooled and exploratory analyses across multiple clinical studies and submission activities (or equivalent)., • Proven ability to work effectively both independently or in a team setting, and to meet set goals by managing own timelines., • Experience in working in cross-functional, multicultural and international clinical trial teams. Competencies • Excellent Verbal, Written, communication and analytical skills with demonstrated Fluency in English., • Strong interpersonal skills and effective leadership., • Strong strategic planning and organizational skills., • Ability to work successfully in a matrix organizational structure., • A solutions-oriented mindset., • Excellent accuracy and attention to detail., • Networking skills and ability to share knowledge and experience amongst colleagues. Presentations of programming techniques at professional conferences is a plus. CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives. CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries. To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit ___ and CSL Plasma at ___. Our Benefits For more information on CSL benefits visit ___. You Belong at CSL At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. To learn more about inclusion and belonging visit Equal Opportunity Employer CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit ___.

The Director, Field Engagement IT Product Manager is a visionary leader responsible for shaping and executing the strategy for enterprise-scale technology platforms that drive commercial and medical field effectiveness and engagement. This role bridges business and technology, ensuring solutions deliver measurable value, support digital transformation, and remain agile in a rapidly evolving biopharma landscape. They will lead cross-functional teams, manage product lifecycles, and champion user-centric design and agile methodologies to deliver scalable, high-impact solutions. This role is accountable not only for technology delivery, but for shaping enterprise-wide business transformation—modernizing operating models, decision-making, and engagement through digital platforms, data, and AI. Success will be measured by measurable improvements in productivity, adoption, compliance, and business outcomes—not output alone. REPORTING RELATIONSHIP Reports To: Executive Director, Commercial I&T Direct Reports: Product Owners, Platform Configuration/Analysts RESPONSIBILITIES 3. Act as a platform steward, accountable for long-term architectural integrity, scalability, and cost efficiency—balancing near-term business needs with enterprise standards and future-state evolution., 4. Manage the full end-to-end product lifecycle, prioritizing features based on business impact, user feedback and emerging technology trends., 5. Ensure robust API integration, adherence to interoperability standards, and implementation of data governance practices to deliver scalable, secure, and compliant solutions., 6. Serve as a senior technology leader embedded with the business units, IT functions, anticipating needs and turning requirements into actionable, secure, and compliant digital products., 7. Own the responsible evaluation, adoption, and scaling of AI and advanced analytics capabilities—partnering with Data, Security, Legal, and business leadership to operationalize AI in compliant, high‑value use cases., 8. Develop and manage strategic relationships with external technology and managed services partners to ensure seamless integration, compliance, and innovation across platforms, 9. Own product financials including vendor strategy, run vs. grow investment decisions, total cost of ownership, and value realization tracking in partnership with Finance and Procurement., 10. Build and mentor high-performing, cross-functional teams, championing agile, DevOps, and user centric design practices, 11. Define and evolve delivery models (product-aligned teams, DevOps, vendor/partner orchestration) to improve speed, quality, and accountability across global teams., 12. Establish and monitor key performance indicators (KPIs) to measure product success, business impact, user adoption, and regulatory compliance., 13. Ensure platforms meet global regulatory, privacy, and cybersecurity standards., 14. Stay ahead of industry trends, regulatory changes, technology innovations, proactively adapting strategies., 15. Drive continuous improvement, operational excellence, and change management initiatives., 16. Serve as a trusted advisor to executive leadership, shaping strategic decisions through data-driven insights, tradeoff analysis, and forward-looking recommendations. JOB SPECIFICATIONS Education • Bachelor’s or advanced degree in Computer Science, Engineering, Information Systems, or related field. Experience • 10+ years experience in product management, application development or digital transformation, • 4+ years in leadership roles., • Pharma/Biotech or similarly regulated environment experience preferred. Additional Comments Skills Required: • Expertise in agile methodologies, SDLC, cloud platforms, AI/ML, data analytics, and cybersecurity., • Exceptional communication, strategic thinking, and stakeholder management skills, • Expertise with cloud-based ecosystems (AWS, Azure) and advanced analytics tools for insights-driven engagement., • Deep understanding of enterprise CRM and engagement platforms in regulated environments (ie., Veeva and Salesforce) Working Conditions • Understands complex problems to collaborate and explore alternative solutions., • Ability to make decisions which have significant impact on the immediate work unit and monitor impact outside immediate work unit., • Fast paced environment with frequent interruptions, • Proven track record of delivering enterprise technology solutions in complex, matrixed environments., • Excellent communication, strategic thinking, and problem-solving skills. Note: All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, disability, veteran status, national origin, or other legally protected classifications. CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives. CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries. To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit ___ and CSL Plasma at ___. Our Benefits For more information on CSL benefits visit ___. You Belong at CSL At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. To learn more about inclusion and belonging visit Equal Opportunity Employer CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit ___.

CSL is looking for a highly technical and detail-oriented leader in the DFIR space that specializes in digital forensics, malware analysis, threat detection, and the fast-paced excitement of supporting incident response activities. As the leader of our Digital Forensics and eDiscovery team, you will be responsible to support and grow a global team, own the strategy and direction for the people, processes, and technology to fulfill your mission, and partner deeply with our Security Operations, Data Loss Prevention, and Threat Intelligence teams to help CSL defend itself from cyber attacks. You will direct the adoption of new tools and technologies to further your goals. The position holder: Leads a global team to apply security incident handling processes for CSL to successfully support the cybersecurity and information security incident response process to: • Prepare for, • Identify, • Contain, • Eradicate The role will lead a global team of digital forensics, incident response and eDiscovery analysts that will: • Work closely with the Director, Security Operations to develop and implement a cybersecurity threat analysis structure of common attack techniques to evaluate an attacker's spread through a CSL system, platform and or network., • Develop and maintain a continuous upskilling program for your team to increase skills and overall capability maturity, • Identify and implement tools to determine attack types and choose appropriate defenses and response tactics for each, • Derive Indicators of Compromise (IOCs) from malicious activity to strengthen incident response, threat detection, and intelligence efforts, • Conduct in-depth forensic analysis of various operating systems, • Examine traffic using common network protocols to identify patterns of activity or specific actions that warrant further investigation, • Detect and hunt for adversary tools, tactics, and procedures (TTPs) across an enterprise environment, • Partner with Compliance, Legal, Privacy, and other teams to perform internal investigations pertaining to eDiscovery matters Demonstrates thought leader-level abilities with, and/or a proven record of success directing efforts in the following areas: Network Analysis Computer Memory Analysis Endpoint Analysis Cyber Incident Lifecycle NIST 800-61 Lead and supervise teams to create an atmosphere of trust and seek diverse views to encourage improvement and innovation, answer questions and provide direction to less-experienced staff, coach staff including providing timely meaningful written and verbal feedback Reports to Executive Director, Enterprise Monitoring & Cyber Resilience Direct Reports – This role will manage a team of Forensics, eDiscovery, Incident Response and Threat Hunting SME’s and may have Project Managers, Project Coordinators, Security Architects, and vendors or managed service providers as direct and indirect reports based on security project portfolio. Main Responsibilities and Accountabilities: Participates in the hiring, growth, and development of junior incident response staff in the areas of threat hunting, forensic analysis, eDiscovery, litigation hold, incident resolution and return to operations. Mentors and directs specially assigned incident response project managers and their teams and program management staff, and actively role models expected project management and leadership behaviors and processes designed to improve project results and the performance of the team. Position Qualifications and Experience Requirements: Required: College degree, preferably in a related technical subject; or advanced degree in business or industry-related subject or equivalent related work experience in cybersecurity and manufacturing. Preferred: An advanced degree (MS) in a relevant discipline (or equivalent) including cybersecurity, management information systems, and related technologies related to manufacturing cybersecurity. Project management certification / training desirable / CISSP, CISM, CISO, GIAC-GCED, GIAC-GCIH, and/or GIAC-CFE certification preferred. Essential Experience: • 8+ years demonstrated experience leading global, multi-functional Digital Forensics/Cybersecurity Incident Response teams (bio-pharma manufacturing environment preferred but not mandatory), • Strong leadership, consultative, communication, and conflict management skills to influence project leaders and stakeholders, including non-specialists, at all levels in the organization and achieve team objectives while maintaining a positive team environment., • The ability to train, mentor, and develop project managers in project management methodologies and their application; the ability to manage in a matrix environment., • The ability to work on complex problems where analysis of situation or data requires an in-depth evaluation of various factors to achieve best results., • The ability to clearly communicate complex issues to senior management so that critical issues are understood quickly and can be addressed immediately., • Strong strategic planning, quantitative, and decision analysis capabilities., • Strong project management and integration skills; ability to coordinate all aspects of a project or program., • Demonstrated experience in developing, managing, and controlling cross functional project budgets., • 8+ years’ experience using a formal project management methodology, techniques and tools., • Experience in biopharmaceutical industry, • Experience in crafting enterprise incident response programs for a global company – process and technical definition. CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives. CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries. To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit ___ and CSL Plasma at ___. Our Benefits For more information on CSL benefits visit ___. You Belong at CSL At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. To learn more about inclusion and belonging visit Equal Opportunity Employer CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit ___.

GENERAL SUMMARY The Director, Commercial and Medical Operations IT Product Manager is a strategic leadership role responsible for driving the vision, roadmap, and delivery of technology platforms that enable operational excellence across commercial and medical domains. This role ensures solutions are innovative, scalable, and compliant, supporting the organization’s transformation and growth. This individual will serve as a key liaison between business stakeholders and I&T teams, ensuring that product strategies align with organizational goals and deliver measurable value. They will lead cross-functional teams, manage product lifecycles, and champion user-centric design and agile methodologies to deliver scalable, high-impact solutions. This role is accountable not only for technology delivery, but for shaping enterprise-wide business transformation—modernizing operating models, decision-making, and engagement through digital platforms, data, and AI. Success will be measured by measurable improvements in productivity, adoption, compliance, and business outcomes—not output alone. REPORTING RELATIONSHIP Reports To: Executive Director, Commercial I&T Direct Reports: Product Owners, Platform Configuration/Analysts RESPONSIBILITIES 1. Lead the design and delivery of platforms for revenue management, contracting, pricing, compliance, meetings, training and other operational domains. Ensure seamless integration with enterprise systems and compliance with regulatory requirements. Enable decision intelligence across commercial and medical operations by integrating data, analytics, and workflow platforms that support compliant, scalable execution., 2. Develop and communicate a strategic product vision, integrating digital, data, automation and AI capabilities to future-proof operations. Partner with executive stakeholders to identify opportunities for digital transformation and innovation., 3. Act as a platform steward, accountable for long-term architectural integrity, scalability, and cost efficiency—balancing near-term business needs with enterprise standards and future-state evolution., 4. Manage the full end-to-end product lifecycle, prioritizing features based on business impact, user feedback and emerging technology trends., 5. Ensure robust API integration, adherence to interoperability standards, and implementation of data governance practices to deliver scalable, secure, and compliant solutions., 6. Serve as the primary liaison between business units and IT, translating requirements into actionable, secure, and compliant solutions. Serve as a senior technology leader embedded with the business units, IT functions, anticipating needs and turning requirements into actionable, secure, and compliant digital products. 7. Own the responsible evaluation, adoption, and scaling of AI and advanced analytics capabilities—partnering with Data, Security, Legal, and business leadership to operationalize AI in compliant, high‑value use cases., 8. Develop and manage strategic relationships with external technology and managed services partners to ensure seamless integration, compliance, and innovation across platforms, 9. Own product financials including vendor strategy, run vs. grow investment decisions, total cost of ownership, and value realization tracking in partnership with Finance and Procurement., 10. Build and develop agile, cross-functional teams, fostering a culture of innovation, accountability, and continuous learning, 11. Define and evolve delivery models (product-aligned teams, DevOps, vendor/partner orchestration) to improve speed, quality, and accountability across global teams., 12. Establish and monitor key performance indicators (KPIs) to measure product performance, business impact, and regulatory compliance., 13. Ensure platforms meet global regulatory, privacy, and cybersecurity standards., 14. Stay ahead of industry trends, regulatory changes, technology innovations, proactively adapting strategies., 15. Drive continuous improvement, operational excellence, and change management initiatives., 16. Serve as a trusted advisor to executive leadership, shaping strategic decisions through data-driven insights, tradeoff analysis, and forward-looking recommendations. JOB SPECIFICATIONS Education • Bachelor’s or advanced degree in Computer Science, Engineering, Information Systems, or related field. Experience • 10+ years experience in product management, application development or digital transformation, • 4+ years in leadership roles., • Proven success delivering enterprise technology solutions in global, matrixed, and regulated environments., • Pharma/Biotech or similarly regulated environment experience preferred. Additional Comments Skills Required: • Expertise in agile methodologies, SDLC, cloud platforms, AI/ML, data analytics, and cybersecurity., • Exceptional communication, strategic thinking, and stakeholder management skills, • Expertise with cloud-based ecosystems (AWS, Azure) and advanced analytics tools for insights-driven operations. Working Conditions • Understands complex problems to collaborate and explore alternative solutions., • Ability to make decisions which have significant impact on the immediate work unit and monitor impact outside immediate work unit., • Fast paced environment with frequent interruptions, • Proven track record of delivering enterprise technology solutions in complex, matrixed environments., • Excellent communication, strategic thinking, and problem-solving skills. Note: All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, disability, veteran status, national origin, or other legally protected classifications. CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives. CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries. To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit ___ and CSL Plasma at ___. Our Benefits For more information on CSL benefits visit ___. You Belong at CSL At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. To learn more about inclusion and belonging visit Equal Opportunity Employer CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit ___.

CSL's R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, we’re building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide. Could you be our next Associate Director, AI & Advanced Analytics? The job is in our King of Prussia, PA or Waltham, MA Office. This is a hybrid position and is onsite three days a week. You will report to the Head of MSPR. You will support the deployment and scaling of AI/ML models, digital agents, and automation solutions across R&D. Contributes to technical delivery, stakeholder coordination, and responsible governance practices to enable innovation and efficiency. Responsibilities: Support development and deployment of AI models, automation scripts, and intelligent agents. Partner with R&D teams and digital leads to identify and prototype use cases aligned to business needs. Contribute to MLOps processes, model documentation, and system validation workflows. Help drive platform integration, compliance tracking, and continuous improvement initiatives. Collaborate on internal capability building (e.g., hackathons, training) and end-user support. Track success metrics such as usage, performance, and value delivered. Qualifications: Bachelor’s or Master’s in Data Science, Computer Science, or a related field. 10+ years of experience in AI/ML, analytics, or automation, preferably in R&D or life sciences. Practical experience building or supporting machine learning pipelines or agent-based tools. Familiarity with MLOps tools, low-code automation platforms, or scripting languages (e.g., Python, R). Strong communication and project coordination skills. #LI-HYBRID CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives. CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries. To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit ___ and CSL Plasma at ___. Our Benefits For more information on CSL benefits visit ___. You Belong at CSL At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. To learn more about inclusion and belonging visit Equal Opportunity Employer CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit ___.

The Senior Engineer, Donor Management Systems supports Plasma Applications by providing full stack application maintenance and operational reporting to achieve business objectives and address any I&T issue that may present in degraded center operations or impact to donor facing services including payments. This role ensures the stability, reliability, and performance of donor‑facing systems by addressing I&T issues that may arise during degraded center operations, including impacts to donor services such as payments, in order to meet business objectives. Reporting Relationships: * Reports to Associate Director, I&T Donor Management Systems * Direct Reports – None Main Responsibilities and Accountabilities: 1. Oversee database performance and configuration to support both application and donor-facing processes, including object implementation, query optimization, and performance tuning., 2. Collaborate on ESB lifecycle management, ensuring channel and component configurations are appropriately aligned to use case and environment., 3. Evaluate emerging technologies to enable integration across medical devices, PDAs, and enterprise applications;., 4. Administer and tune application server environments (e.g., WebLogic) to ensure availability, scalability, and performance across clustered production workloads, 5. Participate in production incident response and on-call rotation, coordinating with cross-functional teams to restore service and document corrective actions, 6. Contribute to capacity planning and cloud modernization initiatives, supporting migration and re-architecture efforts for legacy on-premises workloads, 7. Execute environment changes in line with application lifecycle management and in compliance with CSL operating procedures., 8. Develop and maintain Operational Reporting using JasperSoft or Power BI or similar technology. Position Qualifications and Experience Requirements: Education • Oracle DB, Weblogic experience preferred, Spring Boot, AWS administration a plus, JasperSoft or equivalent, Power Bi or equivalent, familiarity with cloud tooling preferred., • Travel: Potential travel for workshops to support projects. CSL Behring LLC will provide equal employment opportunity for all persons without discrimination on the basis of membership in a legally protected class, including race, color, religion, national origin, gender, age, veteran status, or handicap/disability. CSL Behring is committed to ensuring that diversity and inclusion are a part of our everyday business. CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives. CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries. To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit ___ and CSL Plasma at ___. Our Benefits For more information on CSL benefits visit ___. You Belong at CSL At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. To learn more about inclusion and belonging visit Equal Opportunity Employer CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit ___.

The Director, PEO Partner Management is responsible for leading the management and performance for assigned strategic I&T partner(s). This role acts as the primary liaison between internal stakeholders and strategic partner(s), ensuring alignment with business objectives, driving mutual value, and optimizing partner performance. The Director, PEO Partner Management fosters strong, collaborative relationships, implements standardized governance, and is accountable for the continuous improvement of partner engagement, service delivery, and issue resolution. The Director, PEO Partner Management also facilitates measurement, validation, and reporting of strategic partner SLAs and performance related metrics. The role is central to the evolution from a fragmented, asset/process-based approach to a unified, service-oriented operating model. • Reports to: Executive Director, I&T Partner Ecosystem Office (PEO), • Direct Reports: None (operates in a matrixed environment, collaborating with the PEO team and relevant business and IT stakeholders) Main Responsibilities and Accountabilities: Strategic Partner Relationship Management • Lead management of strategic IT partner(s), ensuring their activities and deliverables are aligned with CSL’s business goals, service expectations and in-line with existing agreements/contracts., • Build and maintain strong, collaborative relationships with strategic partners to drive mutual success and innovation., • Act as the escalation point of contact and liaison between internal stakeholders and partners, facilitating clear communication, risk identification, issue resolution, and strategic alignment., • Foster a culture of transparency, trust, and accountability to drive long-term partner engagement and performance., • Facilitate measurement and reporting of strategic partner(s) performance based on contract SLAs and metrics, ensuring timely and accurate reporting., • Drive strategic partner(s) incentives and penalties based on contractual requirements, supporting accountability and continuous improvement., • Manage escalations and SLA breaches involving strategic partner(s), serving as the escalation point for performance, commercial, and delivery issues, in coordination with Procurement and Legal., • Evaluate effectiveness of SLAs and reporting metrics, and recommend adding, deleting, modifying metrics to align with desired business outcomes., • Manage governance forums, establish calendars and schedules, prepare meeting agendas, and work with partners to provide required reports, dashboards, and meeting minutes., • Ensure timely execution of governance activities, including Quarterly Business Reviews (QBRs), service reviews, and contract renewals., • Align strategic partner delivery with I&T program milestones and business expectations., • Identify and implement value enhancement and innovation opportunities, soliciting input from partners based on market and industry trends and developments., • Coordinate with sourcing, finance, and security teams on partner onboarding/disengagement, management, and compliance, defining expectations and communicating key compliance requirements., • Leverage dashboards summarizing partner performance, governance activities, and risk exposure., • Track partner milestone completion and deliverable acceptance., • Conduct surveys to measure stakeholder and partner satisfaction, using results to inform action plans and improvements., • Perform other related duties as assigned by the PEO Lead. Position Qualifications and Experience Requirements: Education • 10+ years of progressive experience in IT, business, or partner/vendor management roles, preferably in a global, matrixed environment., • Demonstrated experience managing strategic partnerships, driving performance improvement, and resolving complex issues., • Proven ability to build and maintain executive-level relationships with both internal and external stakeholders., • Experience implementing and optimizing partner governance frameworks, performance management processes, and continuous improvement initiatives., • Strategic Thinking: Ability to align partner strategies with enterprise business objectives., • Relationship Management: Skilled at building trust, resolving conflicts, and driving mutual value with strategic partners., • Performance Management: Proficiency in defining, measuring, and reporting on partner performance using SLAs and KPIs., • Change Leadership: Ability to drive adoption of new processes and foster a culture of continuous improvement., • Communication: Strong written and verbal communication skills, with the ability to influence and engage stakeholders at all levels. CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives. CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries. To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit ___ and CSL Plasma at ___. Our Benefits For more information on CSL benefits visit ___. You Belong at CSL At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. To learn more about inclusion and belonging visit Equal Opportunity Employer CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit ___.

CSL is transforming its R&D organization to accelerate innovation and create greater impact for patients. With a streamlined, project-led structure and a focus on collaboration, we're building a future-ready team that excels in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide. Could you be our next Director, Portfolio Development Platform? The job is in our King of Prussia, PA or Maidenhead UK office. This is a hybrid position and is onsite three days a week. You will report to Senior Director, Portfolio Development Platform (TES). Job Purpose You will be responsible for the strategic oversight, operational stability, and continuous advancement of critical biometrics and pharmacometrics technology platforms that enable clinical development execution and decision‑making. This role ensures the reliable operation, scalability, and compliance of core systems supporting Biometrics and Pharmacometrics, including the Clinical Data Repository, Statistical Compute Environments, pharmacometric modeling and simulation platforms, and third‑party data ingestion capabilities. The role requires an understanding of modeling and simulation, precision medicine, and advanced data analysis principles to effectively support pharmacometric and analytical systems. Serving as the primary technical partner to the VP of Biometrics, the Director bridges biometrics and pharmacometrics strategy with technology execution, ensuring platforms are resilient, fit‑for‑purpose, and aligned with CSL’s development objectives. RESPONSIBILITIES AND ACCOUNTABILITIES 1. Provide overall leadership and accountability for development platforms supporting Biometrics and Pharmacometrics. Own the strategic roadmap for delivering systems and service capabilities across multiple business areas., 2. Own the strategic IT relationship with senior business leaders, leveraging a deep understanding of the business strategies, priorities and challenges, to influence alignment of business objectives and its strategy for near and long term. Serve as the primary technical and operational escalation point for the Biometrics and Pharmacometrics organizations, ensuring rapid issue resolution and minimal disruption to clinical, statistical, and modeling activities., 3. Ensure platforms meet regulatory, data integrity, security, and inspection‑readiness requirements, including validated environments to support statistical analysis and pharmacometric modeling in regulated settings., 4. Oversee vendor‑provided technologies and services support including performance management, roadmap alignment, and risk mitigation., 5. Drive lifecycle management of development platforms, including upgrades, enhancements, cloud or high‑performance compute evolution, and reduction of technical debt., 6. Establish and maintain platform governance, documentation standards, and operating processes to ensure long‑term sustainability, audit readiness, and reproducibility of analyses., 7. Support development programs by ensuring analytical readiness, data accessibility, and robust computing environments across studies, programs, and therapeutic areas., 8. Act as the main technology partner and advisor to the VP of Biometrics, translating biometrics and pharmacometrics strategy into scalable, secure, and compliant platform capabilities., 9. Partner closely with Clinical Data Management, Statistical Programming, Pharmacometrics, Data Science, Regulatory, and IT stakeholders to enable seamless data flow and integrated analytical workflows., 10. Champion automation and standardization to reduce manual data handling, accelerate analytical readiness, and improve workflow efficiency across development studies. QUALIFICATIONS: * Bachelor’s degree in Computer Science, Information Systems, Engineering, Biostatistics, Pharmacometrics, Life Sciences, or a related discipline is required. An advanced degree (Master’s or PhD) in a relevant technical or scientific field is preferred, particularly in areas related to biometrics, pharmacometrics, data science, or quantitative sciences. * Minimum 10–15 years of experience supporting clinical development technology systems within the pharmaceutical, biotechnology, or life sciences industry. * Demonstrated experience with clinical systems, statistical computing environments, data integration platforms, and technologies supporting clinical development. * Working knowledge of pharmacometric concepts, modeling and simulation workflows, and the technical requirements needed to support these activities in regulated environments. * Strong experience operating within GxP settings, including system validation, inspection readiness, data integrity, and vendor‑managed solutions. * Ability to travel approximately 10–15%, including domestic and occasional international travel, to support global stakeholders, vendors, and program needs. CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives. CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries. To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit ___ and CSL Plasma at ___. Our Benefits For more information on CSL benefits visit ___. You Belong at CSL At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. To learn more about inclusion and belonging visit Equal Opportunity Employer CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit ___.

The CQA Vendor Oversight and Quality Assurance Lead role will own the quality oversight of external partners supporting R&D and regulated activities (e.g., CROs, CMOs, laboratories, technology vendors). Lead the end-to-end vendor lifecycle—due diligence, qualification, quality agreements, risk based monitoring, issue management, and continuous improvement—ensuring adherence to GLP/GCP/GMP/GVP, data integrity and applicable regulations. This role partners closely with Clinical, Nonclinical, CMC, Safety, Procurement, Legal, and IT to enable compliant, reliable delivery from third parties. Main Responsibilities and Accountabilities: 1. Vendor Lifecycle & Governance • Define and execute risk-based vendor qualification and requalification strategies (paper assessments, remote/onsite diligence assessments, performance reviews)., • In collaboration with R&D/Technical/Legal and QA Functional teams contribute to drafting, negotiating, and maintain Quality Agreements aligned to master service agreements (roles/responsibilities, quality standards, change control, deviation management, data integrity, and inspection support)., • Establish and assure upkeep of vendor KPIs/SLAs, quality dashboards, and governance forums for performance, risk, and remediation tracking., • Lead periodic vendor reviews (e.g., QBRs) as appropriate, ensuring KPIs achieve target level, actions, and corrective and preventive actions (CAPAs) are implemented/verified to assure the overall health of the relationship. 2. Inspections • Support planning of routine GxP audits of CROs, CMOs, labs, and system/service providers; ensuring findings are classified, graded, and reported internally and externally., • Liaise with Vendors/Suppliers to assure corrective and preventative CAPA’s are defined and fit-for-purpose. Perform follow up effectiveness checks., • Coordinate inspection readiness and provide front/backroom support when third party services are in scope, support development of storyboards., • Maintain auditee scheduling, auditor qualification, and audit program metrics. 3. Quality Systems & Compliance • Ensure vendor practices meet GLP/GCP/GMP/GVP, ICH, OECD, ISO, and data integrity principles (ALCOA+) as well as other function specific guidelines, regulations, standards., • Provide input to deviation, complaint, change control, and CAPA processes involving third parties; participate in root cause analysis where appropriate., • Contribute to the Quality Management System (QMS)—procedures, templates, and training—for third party oversight. 4. Risk Management & Continuous Improvement • Lead risk assessments (e.g., risk registers, FMEA) to prioritize controls and monitoring frequency for specific vendors/suppliers., • Drive quality improvements with vendors (process robustness, right first time (cycle time reduction, etc.)., • Analyze trends (audit findings, deviations, complaints) and present management reviews with actionable insights. 5. Cross Functional Partnership • Collaborate with Clinical Operations, Nonclinical, CMC, Safety, Supply Chain, Procurement, Legal, and IT to embed quality requirements in scopes of work and contracts., • Provide guidance during technology transfers, method validations, sample handling, and data flows between sponsor and vendors., • Act as CSL Person-in-Plant as appropriate to provide contemporaneous quality support to CSL specific vendor operations., • Train internal stakeholders on third party quality expectations and best practices. 6. Maintain and share knowledge of Regulations and Requirements • Stay current and up to date with GxP regulations and requirements related to audit management as well as industry/regulatory trends in this area., • Identify and/or create new requirements to ensure a high level of quality and communicate internally. Education Bachelor’s degree in relevant scientific discipline Experience • 3+ years of GxP quality experience with direct vendor/CRO/CMO oversight and/or auditing (GLP/GCP/GMP)., • Demonstrated knowledge of one or more of the following ICH (e.g., E6(R2)/E8(R1)/Q9(R1)), OECD GLP, FDA, EMA, EU Annex 11/21 CFR Part 11, and data integrity (ALCOA+)., • Effective communication and negotiation skills. Competencies • Ability to work with limited supervision and with multinational teams and external suppliers speaking different languages., • Strong analytical and demonstrated problem solving skills, excellent interpersonal/communication/influencing/negotiation skills, and excellent organizational skills with respect to planning / tracking and timelines., • Demonstrated knowledge of QMS implementation and regulatory frameworks., • A strong understanding of the requirements for Quality Assurance in relevant GxP discipline., • Experience in audit/inspection management and processes. Travel: This role will include up to 50% travel CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives. CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries. To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit ___ and CSL Plasma at ___. Our Benefits For more information on CSL benefits visit ___. You Belong at CSL At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. To learn more about inclusion and belonging visit Equal Opportunity Employer CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit ___.

The Opportunity: * The GLP Vendor Oversight and Quality Assurance Lead role will own the quality oversight of external partners supporting R&D and regulated activities (e.g., CROs, laboratories, technology vendors). * Lead the end-to-end vendor lifecycle—due diligence, qualification, quality agreements, risk based monitoring, issue management, and continuous improvement—ensuring adherence to GLP/GCP, data integrity and applicable regulations. * This role partners closely with Research, Clinical, Nonclinical, Procurement, Legal, and IT to enable compliant, reliable delivery from third parties. Main Responsibilities and Accountabilities: 1. Vendor Lifecycle & Governance * Define and execute risk-based vendor qualification and requalification strategies (paper assessments, remote/onsite diligence assessments, performance reviews). * In collaboration with R&D/Technical/Legal and QA Functional teams contribute to drafting, negotiating, and maintain Quality Agreements aligned to master service agreements (roles/responsibilities, quality standards, change control, deviation management, data integrity, and inspection support). * Establish and assure upkeep of vendor KPIs/SLAs, quality dashboards, and governance forums for performance, risk, and remediation tracking. * Lead periodic vendor reviews (e.g., QBRs) as appropriate, ensuring KPIs achieve target level, actions, and corrective and preventive actions (CAPAs) are implemented/verified to assure the overall health of the relationship. 2. Inspections- * Support planning of routine GxP audits of CROs, CMOs, labs, and system/service providers; ensuring findings are classified, graded, and reported internally and externally. * Liaise with Vendors/Suppliers to assure corrective and preventative CAPA’s are defined and fit-for-purpose. Perform follow up effectiveness checks. * Coordinate inspection readiness and provide front/backroom support when third party services are in scope, support development of storyboards. * Maintain auditee scheduling, auditor qualification, and audit program metrics. 3. Quality Systems & Compliance * Ensure vendor practices meet GLP/GCP, ICH, OECD, ISO, and data integrity principles (ALCOA+) as well as other function specific guidelines, regulations, standards. * Provide input to deviation, complaint, change control, and CAPA processes involving third parties; participate in root cause analysis where appropriate. * Contribute to the Quality Management System (QMS)—procedures, templates, and training—for third party oversight. 4. Risk Management & Continuous Improvement * Lead risk assessments (e.g., risk registers, FMEA) to prioritize controls and monitoring frequency for specific vendors/suppliers. * Drive quality improvements with vendors (process robustness, right first time (cycle time reduction, etc.). * Analyze trends (audit findings, deviations, complaints) and present management reviews with actionable insights. 5. Cross Functional Partnership * Collaborate with Clinical Operations, Nonclinical, Procurement, Legal, and IT to embed quality requirements in scopes of work and contracts. * Provide guidance and assure appropriate data flows during technology transfers, method validations, sample handling between sponsor and vendors. * Train internal stakeholders on third party quality expectations and best practices. 6. Maintain and share knowledge of Regulations and Requirements * Stay current and up to date with GxP regulations and requirements related to audit management as well as industry/regulatory trends in this area. * Identify and/or create new requirements to ensure a high level of quality and communicate internally. Education Bachelor’s degree in relevant scientific discipline Experience * 3+ years of GxP quality experience with direct vendor/CRO/CMO oversight and/or auditing (GLP/GCP/GMP). * Demonstrated knowledge of one or more of the following ICH (e.g., E6(R2)/E8(R1)/Q9(R1)), OECD GLP, FDA, EMA, EU Annex 11/21 CFR Part 11, and data integrity (ALCOA+). * Effective communication and negotiation skills. Competencies * Ability to work with limited supervision and with multinational teams and external suppliers speaking different languages. * Strong analytical and demonstrated problem solving skills, excellent interpersonal/communication/influencing/negotiation skills, and excellent organizational skills with respect to planning / tracking and timelines. * Demonstrated knowledge of QMS implementation and regulatory frameworks. * A strong understanding of the requirements for Quality Assurance in relevant GxP discipline. * Experience in audit/inspection management and processes. Travel: This role will include up to 50% travel CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives. CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries. To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit ___ and CSL Plasma at ___. Our Benefits For more information on CSL benefits visit ___. You Belong at CSL At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. To learn more about inclusion and belonging visit Equal Opportunity Employer CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit ___.

The Opportunity: * This role will be responsible for executing the global RDQ audit program within the specified GxP discipline to the accuracy and quality of scientific data, as well as compliance with relevant guidelines, legal requirements, GxPs, and CSL Corporate standards. * The GxP auditor will conduct assigned audits, draft reports, and work collaboratively with the GxP compliance area QA staff to assure categorization, communication, and escalations of audit outcomes. * The program is primarily focused on external audits, and support for internal audits will be required occasionally. * As part of a broader audit team and Community of Practice this role will provide recommendations leading toward continuous improvements, enhancing audit skills, competence, and outputs. The Role: * Support execution of global RDQ audit plans to assess the accuracy and quality of scientific data and/or ensure compliance with relevant guidelines, legal requirements, relevant GxPs, and CSL Corporate requirements. * Assist in the development of a global audit program and schedule, in collaboration with RDQ and functional stakeholders. * Perform external audits of clinical investigator sites, E-Systems, databases, contract CROs/vendors, ECs/IRBs. * Perform self-inspections/audits of internal processes/ procedures relevant to assigned GxP including but not limited to, PV process/procedure, Local and Regional Safety Officers (LSO/RSOs), clinical E-Systems, databases. * Development, review, and issue of Audit Reports outlining the findings categorized according to level of risk/s and corrective and preventive actions (CAPA) recommendations. * Identify non-compliance trends and systematic risks for assigned GxP. * Analyze audit observations, gaps, and systematic issues to help to support continuous improvement within the assigned GxP discipline, as well as affiliates, 3rd party vendors and interfacing functions. * Escalate non-compliances communicating trends to line management, RDQ LT and relevant GxP functional leads. * Support continuous improvement initiatives focusing on processes, procedures, and standard operating procedures (SOPs) for conducting and documenting audits and inspections outcome communications. * Partner with stakeholders to assist in developing and communicating innovative, compliant solutions using a risk-based approach for internal and external inspections with recommended solutions. * Support development of improved principles of auditing and inspections. * Ensure the upkeep accreditation, qualification to perform required inspections and adhere to processes and SOPs to ensure inspectors are trained and accredited. * Maintain and share knowledge of Regulations and Requirements. * Stay current and up to date with GxP regulations and requirements related to audit management as well as industry/regulatory trends in this area. * Identify and/or create new requirements to ensure a high level of quality and communicate internally. Skills & Experience: * BS degree in relevant biological science, science, or related discipline * 3+ years of Quality Assurance experience within a GVP, GCP environment, preferred (other GxP environments will be considered) * Ability to work with limited supervision and with multinational teams and external suppliers speaking different languages. * Strong analytical and demonstrated problem solving skills, excellent interpersonal/communication/influencing/negotiation skills, and excellent organizational skills with respect to planning/tracking and timelines. * Demonstrated knowledge of QMS implementation and regulatory frameworks. * A strong understanding of the requirements for Quality Assurance in relevant GxP discipline. * Experience in audit/inspection management and processes. CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives. CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries. To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit ___ and CSL Plasma at ___. Our Benefits For more information on CSL benefits visit ___. You Belong at CSL At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. To learn more about inclusion and belonging visit Equal Opportunity Employer CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit ___.

OVERVIEW: At Redeemer Health, a career in the rehabilitation therapies is where passion meets purpose. From acute care to pediatrics, sports medicine to home care, we offer a variety of clinical settings across our community health system, which spans across southeastern Pennsylvania and New Jersey. As part of our diverse, inclusive team your professional growth is a priority. At Redeemer Health, you'll find competitive benefits, educational assistance, and a unique onboarding program that ensures your long-term success by immersing you in our mission and celebrated service orientation. Here your career is more than just a job - it's an opportunity to make impactful contributions in healthcare. Together, let's drive excellence in healthcare. SUMMARY OF JOB: $3000 SIGN ON BONUS Holy Redeemer Home Care and Hospice's ability to continue the rich heritage of the Sisters of the Redeemer and care, comfort, and heal in the home is directly related to the talents, motivation and accomplishments of our employees. A primary way staff connect to our mission is by collaborating with all team members in promoting an environment that provides quality, compassionate, holistic, patient-centered care and supports all internal and external customers. Evaluate and treat patients, under orders from the referring physician, through the use of a variety of therapeutic procedures, to restore function, relieve pain, and to improve movement and function. The Physical Therapist functions in accordance with their State Practice Act, as applicable. RECRUITMENT REQUIREMENTS: • Graduate of an APTA approved and accredited college of Physical Therapy., • Excellent oral and written communication and interpersonal skills., • Demonstrate competency in applying principles, methods, materials and equipment used in physical therapy., • CPR required., • Ability to assess patient needs and develop and implement a comprehensive plan of care., • Ability to function as a member of an integrated Healthcare work team., • Able to travel to patient's home within service area., • Able to demonstrate professional procedures in the home care setting., • Able to use office equipment; i.e. tablet, cell phone., • Ability to work flexible hours, with weekends and holidays included. LICENSE AND REGULATORY REQUIREMENTS: • Current license in the state of practice.

OVERVIEW: At Redeemer Health, a career in the rehabilitation therapies is where passion meets purpose. From acute care to pediatrics, sports medicine to home care, we offer a variety of clinical settings across our community health system, which spans across southeastern Pennsylvania and New Jersey. As part of our diverse, inclusive team your professional growth is a priority. At Redeemer Health, you'll find competitive benefits, educational assistance, and a unique onboarding program that ensures your long-term success by immersing you in our mission and celebrated service orientation. Here your career is more than just a job - it's an opportunity to make impactful contributions in healthcare. Together, let's drive excellence in healthcare. SUMMARY OF JOB: $6000 SIGN ON BONUS Holy Redeemer Home Care and Hospice's ability to continue the rich heritage of the Sisters of the Redeemer and care, comfort, and heal in the home is directly related to the talents, motivation and accomplishments of our employees. A primary way staff connect to our mission is by collaborating with all team members in promoting an environment that provides quality, compassionate, holistic, patient-centered care and supports all internal and external customers. Evaluate and treat patients, under orders from the referring physician, through the use of a variety of therapeutic procedures, to restore function, relieve pain, and to improve movement and function. The Physical Therapist functions in accordance with their State Practice Act, as applicable. RECRUITMENT REQUIREMENTS: • Graduate of an APTA approved and accredited college of Physical Therapy., • Excellent oral and written communication and interpersonal skills., • Demonstrate competency in applying principles, methods, materials and equipment used in physical therapy., • CPR required., • Ability to assess patient needs and develop and implement a comprehensive plan of care., • Ability to function as a member of an integrated Healthcare work team., • Able to travel to patient's home within service area., • Able to demonstrate professional procedures in the home care setting., • Able to use office equipment; i.e. tablet, cell phone., • Ability to work flexible hours, with weekends and holidays included. LICENSE AND REGULATORY REQUIREMENTS: • Current license in the state of practice.

OVERVIEW: At Redeemer Health, a career in the rehabilitation therapies is where passion meets purpose. From acute care to pediatrics, sports medicine to home care, we offer a variety of clinical settings across our community health system, which spans across southeastern Pennsylvania and New Jersey. As part of our diverse, inclusive team your professional growth is a priority. At Redeemer Health, you'll find competitive benefits, educational assistance, and a unique onboarding program that ensures your long-term success by immersing you in our mission and celebrated service orientation. Here your career is more than just a job - it's an opportunity to make impactful contributions in healthcare. Together, let's drive excellence in healthcare. SUMMARY OF JOB: $3000 SIGN ON BONUS Holy Redeemer Home Care and Hospice's ability to continue the rich heritage of the Sisters of the Redeemer and care, comfort, and heal in the home is directly related to the talents, motivation and accomplishments of our employees. A primary way staff connect to our mission is by collaborating with all team members in promoting an environment that provides quality, compassionate, holistic, patient-centered care and supports all internal and external customers. Evaluate and treat patients, under orders from the referring physician, through the use of a variety of therapeutic procedures, to restore function, relieve pain, and to improve movement and function. The Physical Therapist functions in accordance with their State Practice Act, as applicable. RECRUITMENT REQUIREMENTS: • Graduate of an APTA approved and accredited college of Physical Therapy., • Excellent oral and written communication and interpersonal skills., • Demonstrate competency in applying principles, methods, materials and equipment used in physical therapy., • CPR required., • Ability to assess patient needs and develop and implement a comprehensive plan of care., • Ability to function as a member of an integrated Healthcare work team., • Able to travel to patient's home within service area., • Able to demonstrate professional procedures in the home care setting., • Able to use office equipment; i.e. tablet, cell phone., • Ability to work flexible hours, with weekends and holidays included. LICENSE AND REGULATORY REQUIREMENTS: • Current license in the state of practice.

OVERVIEW: At Redeemer Health, a career in the rehabilitation therapies is where passion meets purpose. From acute care to pediatrics, sports medicine to home care, we offer a variety of clinical settings across our community health system, which spans across southeastern Pennsylvania and New Jersey. As part of our diverse, inclusive team your professional growth is a priority. At Redeemer Health, you'll find competitive benefits, educational assistance, and a unique onboarding program that ensures your long-term success by immersing you in our mission and celebrated service orientation. Here your career is more than just a job - it's an opportunity to make impactful contributions in healthcare. Together, let's drive excellence in healthcare. SUMMARY OF JOB: $6000 Sign On Bonus Holy Redeemer Home Care and Hospice's ability to continue the rich heritage of the Sisters of the Redeemer and care, comfort, and heal in the home is directly related to the talents, motivation and accomplishments of our employees. A primary way staff connect to our mission is by collaborating with all team members in promoting an environment that provides quality, compassionate, holistic, patient-centered care and supports all internal and external customers. Evaluate and treat patients, under orders from the referring physician, through the use of a variety of therapeutic procedures, to restore function, relieve pain, and to improve movement and function. The Physical Therapist functions in accordance with their State Practice Act, as applicable. RECRUITMENT REQUIREMENTS: • Graduate of an APTA approved and accredited college of Physical Therapy., • Excellent oral and written communication and interpersonal skills., • Demonstrate competency in applying principles, methods, materials and equipment used in physical therapy., • CPR required., • Ability to assess patient needs and develop and implement a comprehensive plan of care., • Ability to function as a member of an integrated Healthcare work team., • Able to travel to patient's home within service area., • Able to demonstrate professional procedures in the home care setting., • Able to use office equipment; i.e. tablet, cell phone., • Ability to work flexible hours, with weekends and holidays included. LICENSE AND REGULATORY REQUIREMENTS: • Current license in the state of practice.

OVERVIEW: At Redeemer Health, a career in the rehabilitation therapies is where passion meets purpose. From acute care to pediatrics, sports medicine to home care, we offer a variety of clinical settings across our community health system, which spans across southeastern Pennsylvania and New Jersey. As part of our diverse, inclusive team your professional growth is a priority. At Redeemer Health, you'll find competitive benefits, educational assistance, and a unique onboarding program that ensures your long-term success by immersing you in our mission and celebrated service orientation. Here your career is more than just a job - it's an opportunity to make impactful contributions in healthcare. Together, let's drive excellence in healthcare. SUMMARY OF JOB: Performs medically prescribed occupational therapy treatments to restore function and prevent disability following injury. CONNECTING TO MISSION: Redeemer Health Home Care and Hospice's ability to continue the rich heritage of the Sisters of the Redeemer and care, comfort, and heal in the home is directly related to the talents, motivation and accomplishments of our employees. A primary way staff connect to our mission is by collaborating with all team members in promoting an environment that provides quality, compassionate, holistic, patient-centered care and supports all internal and external customers. RECRUITMENT REQUIREMENTS: · Graduate of an OTA approved and accredited college of Occupational Therapy. · Excellent oral and written communication and interpersonal skills. · Demonstrate competency in applying principles, methods, materials and equipment used in occupational therapy. · Ability to assess patient needs and develop and implement a comprehensive plan of care. · Ability to function as a member of an integrated Healthcare work team. · Able to travel to patient's home within service area. · CPR required. · Able to demonstrate professional procedures in the home care setting. · Able to use office equipment; i.e. tablet, cell phone. · Ability to work flexible hours, with weekends and holidays included. LICENSE AND REGULATORY REQUIREMENTS: · Valid driver's license. · Current license in the state of practice. EQUAL OPPORTUNITY: Redeemer Health is an equal opportunity employer. We prohibit discrimination in employment due to race, color, gender, religion, creed, national origin, age, sex, sexual orientation, gender identity or expression, disability veteran status or any other protected classification required by law.

The Senior Scientist will play a key role in the development, optimization, transfer, qualification, monitoring, and execution of molecular analytical methods supporting gene therapy process development and/or Manufacturing. This individual will provide technical expertise across early- through late-stage programs, ensuring analytical strategies are scientifically sound, phase-appropriate, and aligned with regulatory expectations. The role includes assay design, troubleshooting, data interpretation, method lifecycle management, and cross-functional collaboration with Process Development and/or Manufacturing, Quality, and GMP testing teams to advance program goals. Primary Responsibilities: • Lead and execute molecular method development, optimization, transfer, qualification, monitoring, and lifecycle management to support gene therapy process development/manufacturing and transfer to GMP testing., • Design, perform, and interpret complex experiments with minimal supervision to evaluate vector genomes and related molecular attributes using nucleic acid–based technologies (qPCR, dPCR, ddPCR)., • Provide robust in-process analytics and product characterization support for analytical assays that support Process Development and/or Manufacturing, including support of investigations and technical troubleshooting., • Generate, analyze, trend, and interpret high-quality data; clearly communicate findings and recommendations to cross-functional stakeholders, • Author and review technical reports, protocols, summaries, and source documentation in compliance with GMP standards and to support regulatory submissions., • Present data and project updates at cross-functional meetings and contribute to scientific discussions and decision-making., • Support analytical method qualification activities, continuous improvement initiatives, and data review processes to ensure scientific rigor and regulatory alignment., • Maintain laboratory instrumentation, ensure proper documentation practices, and oversee organization of reagents, materials, and laboratory records in accordance with quality standards., • Work with molecular assays as a primary responsibility and, as needed, support analytical testing across additional assay platforms (e.g., cell-based, potency, or ELISA assays) to meet program and project needs. Education, Experience, & Qualifications: • Bachelor’s or Master’s degree in Molecular Biology, Biochemistry, Cell Biology, Immunology, or related discipline with 6–10 years of relevant industry experience, or a PhD with 3–5 years of industry experience preferred., • Demonstrated experience in development, optimization, transfer, and execution of molecular analytical methods, particularly PCR-based assays (qPCR, dPCR/ddPCR) for nucleic acid quantification and characterization., • Experience supporting gene therapy programs, including molecular assays for vector genome titer, residual DNA analysis, and other nucleic acid–based characterization methods., • Strong expertise in assay troubleshooting, experimental design, and data analysis to support process development, method qualification, and product characterization

The Associate Scientist will execute in-process analytical testing, assay development, and GMP testing when needed for gene therapy products, collaborating with a multidisciplinary Process Development Team, GMP testing team, Quality Assurance, and Manufacturing team. There are current openings in cell and molecular biology–focused disciplines. Primary Responsibilities • Perform laboratory testing in a research and development setting., • Work cross-functionally with scientists and technical staff to support assay execution for gene and cell therapy programs., • Carry out a range of cell-based, molecular biology, and analytical techniques., • Plan and conduct experiments with guidance, ensuring alignment with project goals and timelines., • Draft and support development of test methods for standard operating procedures and regulated laboratory environments., • Execute method development, optimization, qualification, and routine sample analysis., • Summarize findings and present technical data to internal stakeholders., • Maintain thorough and compliant laboratory documentation in line with established procedures and good laboratory practices., • Capture, analyze, and manage experimental data using appropriate systems and tools., • Support general lab operations, including organization, equipment upkeep, and inventory management., • Apply analytical techniques to evaluate and characterize viral vector-based materials., • Perform testing to support process development activities, investigations, and product characterization efforts., • Partner with cross-functional teams to assess product quality attributes and process-related impurities in cell and gene therapy products. Education, Experience, & Qualifications • Bachelor’s or Master’s degree in Biology, Biochemistry, Molecular Biology, Immunology, or a related scientific discipline., • Approximately 1–4 years of relevant laboratory experience in biotechnology, pharmaceuticals, or a related field., • Hands-on experience with analytical and characterization methods such as plate-based assays, immunoassays (e.g., ELISA), and nucleic acid–based techniques (e.g., qPCR, digital PCR) is preferred., • Familiarity with mammalian cell culture, cell-based assays, and aseptic laboratory techniques is strongly preferred.

Title: Process Lead – CQV & Automation Location: Philadelphia, PA Duration: Longterm Contract (likely through 2031) Start: Rolling Starts (ongoing need) Greenfield CAR-T Manufacturing Facility *Skills, experience, and other compensable factors will be taken into account when determining pay rate. The pay range provided in this posting is a reflection of a W2 hourly rate. We are seeking an experienced Process Lead with deep CQV and Automation expertise to support a greenfield CAR-T manufacturing facility. This is a high-impact role responsible for driving process validation strategy, supporting automation integration, and ensuring compliance in a cutting-edge cell therapy environment. This is an exciting opportunity to play a key role in building a facility from the ground up and shaping next-generation manufacturing processes. Key Responsibilities • Lead process engineering activities for a greenfield cell therapy manufacturing facility, • Oversee the full CQV lifecycle (Commissioning, Qualification, Validation – IQ/OQ/PQ), • Drive process performance qualification (PPQ) and validation strategies, • Partner cross-functionally with Automation, MSAT, QA, and Engineering teams, • Support automation system integration (DeltaV, PLC, SCADA) aligned with process requirements, • Review and approve validation protocols, reports, and technical documentation, • Ensure compliance with cGMP, FDA, and regulatory standards, • Identify and mitigate process and system risks, • Provide technical leadership and guidance across project teams Required Qualifications • Bachelor’s or Master’s degree in Chemical Engineering, Biotechnology, or related field, • 12+ years of experience in biopharma / life sciences, • Strong hands-on experience with CQV in GMP-regulated environments, • Experience with automation systems (DeltaV, Rockwell, Siemens, PLC/SCADA), • Proven experience supporting process validation (IQ/OQ/PQ, PPQ), • Excellent communication and cross-functional collaboration skills Preferred Qualifications • Experience supporting greenfield / facility startup projects, • Background in CAR-T, cell therapy, or gene therapy manufacturing, • Experience with Kneat or other electronic validation systems, • Strong understanding of data integrity and 21 CFR Part 11

Description: Senior Product Manager, Global Marketing - CNS Cancers Chesterbrook, PA / Full Time / Exempt / Permanent At Novocure, we are patient-forward, aspiring to make a difference in cancer. Together with our patients, we strive to extend survival in some of the most aggressive forms of cancer by developing and commercializing our innovative therapy. WHAT YOU'LL DO • Support the Director, Global Marketing CNS Cancers in preparation for the global launch in brain metastases for non-small cell lung cancer (NSCLC), • Help lead the development and execution of the global launch plan, including launch sequencing, readiness milestones, and cross-functional alignment, • Develop global positioning, messaging, value propositions, and launch templates for regional and local markets, • Lead development of the core global marketing campaign and creative assets for the brain metastases indication, • Partner closely with the Global Core Launch Team and collaborate with Regional Marketing, Medical Affairs, Patient Experience, Clinical Development, and Regulatory teams, • Track competitive intelligence and assess emerging therapies in the brain metastases landscape, • Guide regional and local markets to ensure consistency in branding and communications, • Share best practices across regions and support global-to-local execution, • Participate in strategic and business planning for current and future CNS indications, • Apply creativity, innovation, and out-of-the-box thinking to solve complex business challenges ABOUT YOU • Bachelor's degree required (or equivalent combination of education and experience), • MBA or advanced scientific degree preferred, • Minimum of 5 years of experience in in-line product marketing or global marketing, preferably in oncology, • Strong understanding of healthcare product marketing regulations and processes, • Proven ability to build and maintain partnerships with key opinion leaders, • Ability to work independently and collaboratively in a global matrix environment, • Strong written, verbal, presentation, and influencing skills, • Experience supporting global oncology product launches, • Experience working with regional and country marketing teams WHAT WE OFFER The pay range which Novocure expects to pay for this role at the time of this posting is $132,000- 221,000/yr. This position may also be eligible for an annual bonus and restricted stock unit grant in addition to a full range of benefits. Individual compensation within this range depends on a variety of factors, including, but not limited to, prior education and experience, job-related knowledge and skills demonstrated. NOVOFLEX We offer a flexible, trust-based hybrid working model for most of our office-based roles. Employees are asked to be in the office an average of three days per week, with the flexibility to choose which days' work best for them. We understand that life is not always predictable, so if you need to adjust your schedule, such as leaving early or starting late occasionally, we trust you to balance your time in a way that works for both you and Novocure. ABOUTNOVOCURE: Novocure is a company with a powerful mission, to extend the lives of people living with some of the most aggressive forms of cancer. Here your work will have a direct impact on patients and those who care about them. Join a team of passionate, collaborative people who support each other, challenge one another, and innovate together. Here, you'll connect, grow, and make a real difference. We're a company with the drive of a startup and the strength that comes with 25 years of success. Novocure operates at a rare crossroad, where advanced medical technology converges with cutting-edge biotechnology. We are the only company to develop and commercialize Tumor Treating Fields (TTFields), a proprietary, groundbreaking therapy designed to disrupt cancer cell division. With us you will find a unique combination of laboratory research work alongside engineering development of advanced technologies. This fusion of disciplines positions us as true pioneers in oncology innovation, leading a new frontier in the treatment of aggressive cancers. Our patient-forwardvalues • innovation, • focus, • drive, • courage, • trust, • empathy Novocure is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state, or local law. We actively seek qualified candidates who are protected veteran and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act. Novocure is committed to providing an interview process that is inclusive of our applicant's needs. If you are an individual with a disability and would like to request an accommodation, please email ___ If you're excited about this role, please apply. #LI-ER

Description: PharmD Portfolio Strategy Fellow Hybrid / Full Time (1 -Year Fellowship) / Chesterbrook, PA At Novocure, we're working to extend the lives of patients battling some of the most aggressive cancers. As a PharmD Portfolio Strategy Fellow, you'll play a meaningful role in shaping how innovative therapies are developed, positioned, and brought to patients. This fellowship offers a unique opportunity to gain hands-on experience at the intersection of clinical development, portfolio strategy, and commercialization within a fast-growing oncology-focused medical device company. ABOUT THE ROLE We are seeking a PharmD Portfolio Strategy Fellow to support strategic initiatives across our oncology portfolio. This role is designed to provide broad exposure to how clinical insights translate into commercial strategy and long-term portfolio planning. You will partner with cross-functional teams across Clinical, Medical Affairs, Marketing, Market Access, and Regulatory to support key business decisions and drive forward high-impact initiatives. This fellowship is offered in collaboration with the Industry Pharmacists Organization (IPhO), providing access to a national network of fellows and professional development opportunities. WHAT YOU'LL DO • Support portfolio strategy and planning initiatives to advance pipeline and commercial goals, • Contribute to clinical and scientific evaluations, including literature reviews and study assessments, • Coordinate and support cross-functional projects, ensuring alignment on deliverables and timelines, • Analyze interdependencies across functions and their impact on product strategy, timelines, and risk, • Collaborate with internal stakeholders across Clinical, Medical Affairs, Marketing, Market Access, and Regulatory, • Manage relationships with external partners and support execution of strategic initiatives, • Assist in evaluating future indications and long-term portfolio opportunities, • Participate in IPhO programming and co-lead a National Fellows Council (NFC) committee ABOUT YOU You are a motivated and intellectually curious PharmD graduate who is eager to apply your clinical knowledge in a strategic, business-focused environment. You enjoy working across teams, solving complex problems, and contributing to initiatives that have a direct impact on patients. You bring strong communication skills, attention to detail, and the ability to manage multiple priorities in a fast-paced setting. Minimum Qualifications • Doctor of Pharmacy (PharmD) degree from an accredited institution, • Demonstrated leadership through academic, extracurricular, or professional activities, • Strong written and verbal communication skills, • Ability to work both independently and collaboratively, • Strong organizational and project management skills Preferred Qualifications: • Prior internship or rotation in biotechnology, pharmaceutical, or medical device industry, • Interest in oncology, clinical development, or portfolio strategy, • Experience working on cross-functional or team-based projects, • Ability to synthesize complex information into clear insights HOW YOU'LL WORK • Hybrid work model with in-office collaboration in Wayne, PA, • Exposure to cross-functional teams and senior stakeholders, • Fast-paced, high-impact environment with meaningful project ownership, • Opportunity to develop both strategic thinking and execution skills, • Travel up to ~30%, including conferences and internal meeting FELLOWSHIP DETAILS • 1-year fellowship in partnership with IPhO, • Salary of $80,000, • Start date: Summer 2026, • Participation in national fellowship programming and networking opportunities ABOUT ___NOVOCURE: Novocure is a company with a powerful mission: to extend the lives of people living with some of the most aggressive forms of cancer. We are pioneers in oncology innovation, developing Tumor Treating Fields (TTFields), a proprietary therapy designed to disrupt cancer cell division. Here, you'll work at the intersection of science, technology, and patient care - collaborating with passionate teams committed to making a real difference. Our patient-forward values • innovation, • focus, • drive, • courage, • trust, • empathy #LI-RJ1 Novocure is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state, or local law. We actively seek qualified candidates who are protected veteran and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act. Novocure is committed to providing an interview process that is inclusive of our applicant's needs. If you are an individual with a disability and would like to request an accommodation, please email ___ If you're excited about this role, we encourage you to apply.

Job DescriptionDescription: About Century Therapeutics Century Therapeutics (NASDAQ: IPSC) is a biotechnology company advancing a pipeline of induced pluripotent stem cell (iPSC)-derived cell therapies with the potential to meaningfully address autoimmune diseases, including type 1 diabetes, and cancer. The company’s therapies are derived from its iPSC cell foundry and leverage its novel immune evasion engineering technology, Allo-Evasion™. Century believes its approach to developing off-the-shelf cell therapies will expand patient access and provide advantages over existing cell therapies which will ultimately advance the course of care. Role The Senior Engineering Associate/ Associate Engineer, Manufacturing Science and Technology will be responsible for developing/ implementing and executing manufacturing processes for Century’s cellular therapy programs. The candidate will be expected to receive process tech transfers, implement them into a GMP manufacturing facility, and be a hands-on operator for the Phase I manufacturing campaign. This role is also responsible for ongoing process development on these programs including bioreactor selection, evaluation, scale up and characterization. This includes designing and executing studies, analyzing data and presenting results under the supervision of a team leader. This role requires extensive collaboration with internal and external teams. The successful candidate will need strong scientific background, interpersonal skills, and ability to work collaboratively with other groups across organizations. The expected annual salary range for this role is approximately $110,000 - $123,000 depending on experience and level of role ultimately offered. Additional benefits offered include but are not limited to an annual performance-based bonus (prorated by start date), medical, dental, and vision insurance, matching 401K plan, and 20+ days per-year of PTO (prorated by start date). Requirements: • Receive tech transfers from development into GMP and from other sites., • Implement and run cell processes into GMP manufacturing., • Assist in developing, executing, and documenting process development experiments., • Operate and maintain lab equipment., • Author technical documents (batch records, SOPs, reports, etc.)., • Support preparation of CMC documents for regulatory filings., • A BS or MS degree in biochemical, chemical, biomedical engineering or other related field., • Senior Engineering Associate: 2-4 (BS) or 0-2 (MS) years of relevant professional experience., • Knowledge of cell culture and aseptic technique., • Strong scientific background., • Experience with bioreactors a plus. Century Therapeutics Inc. is an Equal Employment Opportunity/Affirmative Action Employer - Minority/Female/Disability/Veteran. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, or veteran status or any other characteristic protected by federal, state, or local law.

Job Description When you join our team, you’re not just starting a job, you’re becoming part of a compassionate community dedicated to making a meaningful difference every day. If you’re driven by purpose, committed to service, and ready to empower others, we invite you to build your career with us. Position Type: FTE (37.5 hours per week) Starting Pay Range: $32.00 per hour PURPOSE: Under the supervision of the CHS/IDD Director, the nurse supervises medication administration, reviews medical records/appointments, writes and maintains medical histories, follows up on Dr.’s orders, diagnosis and treatment plans as needed, Support Plans as needed, coordinates overall medical participation of each resident including, but not limited to, primary physician, neurology, physical therapy, psychiatric and all other disciplines. PURPOSE: Under the supervision of the Community Home Services, Intellectual Disabilities Division Director, the nurse supervises medication administration, reviews medical records/appointments, writes and maintains medical histories, follows up on Doctor’s orders, diagnosis and treatment plans as needed, Support Plans as needed, coordinates overall medical participation of each resident including, but not limited to, primary physician, neurology, physical therapy, psychiatric and all other disciplines. FUNCTIONS: 1. The nurse is responsible for the overall planning and coordination of the physical health of the CHS(Community Home Services) residents, including:, 2. Visiting each resident on the caseload in their home at least 1 time per month, and completing a nursing note, documenting the visit. In addition, completing and documenting a medication check for each person visited., 3. Reviewing all medical consults and physicals. Follow up with doctor if necessary. Upon review, emailing detailed summaries of documentation received, indicating follow up needed and ensuring that all follow up medical appointments are made., 4. Updating Lifetime Medical Histories annually and as needed when a major medical change occurs. LMH must be updated within one week of any major medical change, including diets, mobility, adaptive equipment, etc., 5. Developing and participating in on-going training for staff on medical issues. Immediate training is needed for any major medical change, including diets, mobility, adaptive equipment, seizure rescue medication etc., 6. Attending all ISP(Individual Support Plan), QEST (Quality Enhancement Support Team), and SIS (Supports Intensity Scale) meetings., 7. Acting as liaison to hospitals, nursing homes, etc., to ensure proper medical follow-through for people using those facilities. Follow up with Physical/Occupational Therapy/Visiting nurses if a resident is receiving these services., 8. Visiting hospitalized individuals within 24 hours of admittance or no later than Monday noon if the admittance occurs on the weekend, speaking with hospital for updates, and participating in discharge planning. Completing a home visit within 24 hours of discharge., 9. Taking verbal orders from doctors, ensuring new prescriptions are filled and delivered to the home and transcribed on the MAR(Medicine Administration Record). If you are sending an email and do not receive a response, please follow up with a phone call to the Program Manager or go to the home and ensure the medication arrived. Also, please make sure it was transcribed., 10. Communicating with the pharmacy as the point of contact for all pharmacy related issues, and going to the home to update MAR (Medical Administration Record) if a verbal order is received., 11. Completing the HRST(Health Risk Screen Tool) Clinical Review for everyone on caseload., 12. Participating in scheduled bi-weekly supervision with the Intellectual Developmental Disabilities Director or Assistant Director., 13. Maintain the agency-issued cell phone and respond to calls within 30 minutes. The on-call supervisor will contact the on-call nurse with questions related to the emergent care of the client and confirm next steps., 14. Participate in a rotating on-call schedule with other nursing staff., 15. Maintaining open line of communication with supervisor, program managers, family members, and all team, members., 16. When the Nursing Assistant is unavailable, appointments will not be delayed if they needed to be scheduled within a week or month.. Nursing staff will assume assigned responsibilities for scheduling appointments and other essential duties to ensure uninterrupted care., 17. Completing IDD(Intellectual Developmental Disability) Annual Training Plan as required per quarter before the due date., 18. Adhering to safe practices., 19. Completing other duties as assigned., 20. Functioning in full compliance with all applicable policies and procedures, federal, state, and local laws Interact’ s Code of Conduct. Must participate in reporting suspected violations of the Compliance Program or applicable laws or regulations to supervisors/managers/Directors or to the Compliance Officer. QUALIFICATIONS: 1. Pennsylvania Licensed Practical Nurse or Registered Nurse Certificate., 2. Two (2) years’ nursing experience, preferably in a residential home environment., 3. An examination statement which indicates that the employee is free from communicable disease at time of employment and every two (2) years thereafter, which includes TB testing (PPD and/or chest X‑ray)., 4. Clearance in accordance with PA Act 33 & 80., 5. Must have a valid Childline, PA Criminal History, FBI Clearances prior to seeing clients. Interact Offers Benefits to Their Employees Who Work 30+ Hours. These Benefits Include: 1. Paid training, 2. Referral bonus, 3. Tuition reimbursement, 4. 401k, 5. Health insurance, 6. Paid time off, 7. Vision insurance, 8. Health savings account, 9. Dental insurance We prohibit discrimination and harassment of any kind based on race, color, M/F, non-binary, veterans, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or other protected characteristics as outlined by federal, state, or local laws.

Job Description We're in this for the greater good at ParetoHealth. Our mission is collective greatness, nothing less will do. Our team is a single force united in the drive to transform employee health benefits. The company was founded in 2011 to help small and medium-sized businesses fight the rising cost of employee health benefits. We blazed the trail with financing innovations that reduce the risks in self-insurance and deliver significant savings—and we continue to lead with a growing ecosystem of partners and world-class cost control solutions. But success is measured by more than dollars alone and we measure ours by the good that comes from knowing that every client and all their employees can count on effective, affordable healthcare for years to come. Please note that ParetoHealth does not provide employment visa sponsorship for this position. Candidates must be authorized to work in the United States without sponsorship both now or in the future. Position Summary: ParetoHealth has built the strongest stop-loss platform in the market. Our continued growth now depends on fully integrating and elevating the ecosystem that surrounds it — medical cost containment, pharmacy (PRxC), and our preferred TPA network. We are seeking a senior executive to own the strategy, performance, and evolution of the Savings Engine ecosystem end-to-end. This is a platform-level leadership role with full accountability across partner strategy, performance, and expansion. Key Responsibilities: • Proactively manage risk exposure within existing partnerships (performance, integration, economic sustainability)., • Lead renegotiation, restructuring, or exit decisions where warranted., • Ensure every ecosystem component continues to justify its economic and strategic role.Offensive Strategy, • Identify and prioritize high-impact new areas (e.g., cell & gene therapy, infusion management, specialty risk, site-of-care optimization)., • Develop and execute sequencing for expansion. • Head of Point Solution Partnerships, • Head of PBM Strategy & Partnerships, • Set strategic direction and execution priorities, • Establish measurable KPIs, • Drive performance discipline, • Ensure cross-vertical alignment You are responsible for building the right team to support the platform. 3. Full Executive Accountability for Partner Portfolio You hold executive accountability for all ecosystem partners — existing and future — across: • Point solutions, • PBMs, • Executive-level relationship ownership, • Performance oversight and escalation, • Renewal and renegotiation strategy This includes: • Partner tiering and segmentation, • Formal launch and GTM integration processes, • Performance scorecards and QBR discipline, • Renewal governance, • Escalation frameworks Responsibilities include: • Contractual and operational performance standards, • Implementation quality and reporting consistency, • Renewal coordination and discipline, • Integration with PRxC and medical solutions • Clarify and strengthen the Savings Engine narrative, • Improve ecosystem simplicity and positioning, • Drive increased adoption and utilization across members, • A clearly articulated and executed 12- and 36-month ecosystem roadmap, • Multiple strategic initiatives advancing simultaneously, • Fully institutionalized partner management discipline, • Strong, accountable TPA and PBM performance, • Increased Savings Engine adoption and utilization, • Clear market perception of Pareto as a coordinated cost containment platformRequired Skills & Qualifications:, • 10-15 years relevant experience within the healthcare/insurance space, • Deep experience in self-funded employer health benefits, • Strong understanding of stop-loss economics and claims dynamics, • Experience leading across PBMs, TPAs, and medical cost containment ecosystems, • Proven ability to scale partner portfolios and teams, • Executive presence with internal and external stakeholders Perks & Benefits: • Fully paid medical, dental, and vision benefits., • Flexible PTO, • 401k company contribution, • Tuition reimbursement, • Professional development allowance, • Transportation allowance and daily parking reimbursement The drive to learn, to improve, and to deliver outstanding value every day. See the field The ability to see the big picture and prepare to meet tomorrow's needs. Get it done right The passion to produce at higher rates and to the highest standards. For the greater good A united community creating better health benefit solutions for all. Please note that any communication from our recruiters and hiring managers at ParetoHealth about a job opportunity will only be made by a ParetoHealth employee with an @paretohealth.com address. ParetoHealth does not conduct text message or chat-based interviews. Any other email addresses, agencies, or forums may be phishing scams designed to obtain your personal information. We will not ask you to provide personal or financial information, including, but not limited to, your social security number, online account passwords, credit card numbers, passport information, and other related banking information until we begin onboarding activities, which will be coordinated by a member of the ParetoHealth People Ops Team with an @paretohealth.com email address.Disclosures:ParetoHealth is an Equal Opportunity Employer and does not discriminate on the basis of race, color, religion (creed), gender, gender expression, age, national origin (ancestry), disability, marital status, sexual orientation, or military status, in any of its activities or operations. These activities include, but are not limited to, hiring and firing of staff, selection of volunteers and vendors, and provision of services. We are committed to providing an inclusive and welcoming environment for all members of our staff, clients, volunteers, subcontractors, vendors, and clients.California Applicants: See Pareto's CCPA Notice of Collection for California Employees and Applicants for information about how Pareto Captive Services, LLC, Pareto Health, LLC, and Pareto Underwriting Partners, LLC, together with their respective subsidiaries (collectively, "Pareto") collects and uses personal information submitted by employment applicants.

Job DescriptionDescription: Century Therapeutics (NASDAQ: IPSC) is a biotechnology company advancing a pipeline of induced pluripotent stem cell (iPSC)-derived cell therapies with the potential to meaningfully address autoimmune diseases, including type 1 diabetes, and cancer. The company’s therapies are derived from its iPSC cell foundry and leverage its novel immune evasion engineering technology, Allo-Evasion™. Century believes its approach to developing off-the-shelf cell therapies will expand patient access and provide advantages over existing cell therapies which will ultimately advance the course of care. Position Summary We are seeking a highly motivated and innovative co-op to support development, optimization, and fit-for-purpose qualification of flow cytometry based and molecular ddPCR assays for Phase 1 clinical studies in cell therapy, following FDA guidance for early-phase bioanalytical method development. In this role, the co-op will work closely with a small team of scientists to develop robust assays to assess clinical assets’ therapeutic performance. The student will gain hands-on experience with immune cell culture, flow cytometry, and a range of in vitro functional assays used to assess cell therapy products. These biomarker approaches will be examined through the lens of bioanalytical method industry standards. The co-op will also contribute to data analysis, interpretation, and presentation of findings to internal teams. This opportunity is ideal for a candidate who is enthusiastic about immunology, cell therapy, and translational research, and who is eager to build technical and analytical skills in a biotech environment focused on advancing innovative therapies toward the clinic. This role is full time at 40 expected hours a week in our Watertown, MA facility. The anticipated start is early June and end in mid-December. The pay offered is $23.00 - $25.00/hr. depending on degree program. Responsibilities • Support development, optimization, and fit-for-purpose qualification of both flow cytometry–based and molecular ddPCR assays for Phase 1 clinical studies, following FDA guidance for early-phase bioanalytical method development., • Gain exposure to regulatory decision-making in early clinical development by contributing assay data and qualification data packages., • Culture and maintain tumor cells along with processing of PBMCs for assay controls., • Analyze, interpret, and present experimental data to internal teams., • Collaborate cross-functionally with scientists across all levels to advance internal research programs., • Maintain accurate experimental records in an electronic lab notebook and contribute to supporting documentation., • Participate in shared lab responsibilities to help maintain a productive research environment.Requirements:, • Currently enrolled in either an undergraduate or graduate level program in the biological sciences., • Experience with mammalian cell culture and aseptic technique, • Flow cytometry experience preferred, • Familiarity with scientific software such as FlowJo, GraphPad Prism, and Microsoft Office, • Strong organizational skills and attention to detail, • Ability to work independently and think critically about experimental design and data, • Motivated, curious, and passionate about immunology and translational science

Job Description Overview Join a Leader in Home Healthcare At Rotech Healthcare Inc., we’re more than a medical equipment provider—we’re a trusted partner in patient care. As a national leader in ventilators, oxygen therapy, sleep apnea treatment, wound care, diabetic solutions, and other home medical equipment, we empower patients to manage their health from the comfort of home. With hundreds of locations across 45 states, our team delivers high-quality products, exceptional service, and compassionate support that helps patients live more comfortably, independently, and actively. Whether you're a clinician, technician, or healthcare administrator, your work at Rotech directly improves lives. Explore more about our mission and services at Rotech.com. Responsibilities Job Title: Account ExecutiveWe’re a national provider focused on delivering essential respiratory therapies, providing wound care, and diabetes management. We need skilled, motivated Account Executives to help us grow. If you're passionate about making a meaningful difference while earning top-tier rewards, this opportunity is for you. Essential Job Duties and Responsibilities (Reasonable accommodations may be made to enable individuals with disabilities to perform these essential functions. Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice.) • Identify, develop, and grow referral relationships within hospitals, physician clinics, and other service areas., • Educate healthcare providers about Rotech's products, services, and value-based care., • Own your rural territory: prospect, present, and close new accounts, • Partner with our local team to ensure seamless service, • Report sales activity and territory trends to management via call planner, • In person visits to referral sources within the assigned territory Performs other duties as assigned What’s In It for You • Uncapped Commission – High earnings potential based entirely on performance, • Quarterly Bonuses – Get rewarded for exceeding goals, • Competitive Base Salary – We recognize and value your expertise, • Mileage Reimbursement – Support provided for rural travel, • Company-provided cell phoneThis is more than a sales job—it's a chance to change lives. If you're ready to drive your future while helping patients access the care they deserve, apply today. Qualifications Employment is contingent on • Background check (company-wide). Results will not be used automatically to disqualify individuals. Instead, the Company will conduct an individualized assessment that considers the duties of the position, the nature and timing of the offense, and any evidence of rehabilitation, in accordance with applicable laws., • Drug screen (when applicable for the position), • Compliance with healthcare facility credentialing process (when applicable for the position), • Four year college degree preferred or equivalent combination of education and experience, • Experience in respiratory or medical sales is preferred, • Leadership Experience in other areas or fields, • Proven Sales Performer – 2+ years in B2B or healthcare sales preferred however, new college graduates are welcome to apply., • Independent & Resourceful – You thrive on autonomy and accountability, • Excellent Communicator – Ability to simplify complex topics and build trust, • Willingness to Travel – Position requires in-person visits throughout your assigned rural territory, • Motivated and self driven, with a proven history of success in sales, • Desire to work in an environment that rewards for top performance, • Strong Team player, • Demonstrated ability to build and maintain solid working relationships with internal and external customers geographically located within the assigned territory, • Highly organized, strong interpersonal skills, • Effectively communicate in English; both oral and written, • Interpret a variety of communications (verbal, non-verbal, written, listening and visual), • Maintain confidentiality, discretion and caution when handling sensitive information, • Multi-task along with attention to detail, • Self-motivation, organized, time-management and deductive problem solving skills, • Email transmission and communication, • Internet navigation and research, • Microsoft applications; Outlook, Word and Excel, • Lift and carry office equipment at times, • Requires sitting, walking, standing, talking and listening, • Requires close vision to small print on computer and/or tablet and paperwork

Job Description Life Science Software Sales Location: Greater Philadelphia Area Territory- Mid-Atlantic to begin with but can grow larger in time Title: Business Development Manager or Account Development Specialist depending on experience. Product or Service: Cell culture software service and platform Join a life science company that is aiming to revolutionize cell culture efficiencies by empowering scientists with digital cell culture manufacturing and lab execution solutions to build the future of Cell Therapy, Gene Therapy, and Cell Culture. This Saas platform defines and manages all assay workflows, activities, equipment, materials, personnel, data/calculations, and projects in assay development and biomanufacturing at all stages of development. The compliance and regulatory scope span early Research and Development, GLP testing, and GMP manufacturing, and FDA Compliance 21 CFR Part 11. The integrated platform has active configured workflow support, supports tech transfer and scalability across multiple R&D stages, and provides real-time analytics and its dashboards provide greater visibility into projects across multiple sites. Position Summary: We are seeking energetic, self-reliant individuals who can translate innovative solutions into sales. Ideal candidates will have a successful track record in territory development and demonstrated sales results. This position is an ideal opportunity for individuals who demonstrate the ability to effectively manage work independently and can travel. The business development manager will have broad knowledge in the area of cell culture. Additional training will be provided. Key Responsibilities: * Introduce/Present SAAS solutions while discerning client’s needs and presenting solutions with intelligence and originality. * Support high growth potential region by organizing and following up on leads, cold calling in person and by phone, meeting with customers, writing quotes, price lists, and contracts. * Develop and execute a regional business plan, sell and promote company software services and cloud solutions. * Organize product demonstrations for rapid instrument adoption. * Ability to work independently and as part of a team towards common goals. * Analyze market trends, customer requirements, and competitive strategy, and identify opportunities for increasing customer and business value through product differentiation * Development of new business through excellence in cold calling, qualifying, discovery, online demonstrations, and contract negotiations. * Relationship development with decision-makers at cold call accounts. * Develop go-to-market campaign strategies in the given territories. Requirements: * Sales experience with software platforms, life science capital equipment with software add ons, technical platforms, SAAS (software as a service), or PAAS (platform as a service). * Ability to generate and follow up on leads to close business. * Ability and enthusiasm to work within a startup environment which means wearing multiple hats and finding non-linear solutions with minimal supervision. Education * Bachelors, Masters, or Ph.D. in Business, Life Science, Computer Science or equivalent required. * Ideally, we would like someone with experience in cell culture to be able to understand the utilization of the platform, however we will train the right candidate.