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We are seeking outstanding scientists who combine scientific excellence with a clear vision for advancing innovative research at the Quadram Institute, leveraging our substantial capabilities and expertise to help consolidate the Institute as a global leader in food-microbiome research for life-long

As a Global Study Manager you will be assigned to pRED early phase clinical studies, and as part of a cross-functional study team, you will be responsible for delivering study management and clinical operations activities under the direction and leadership of a Study Management Team Leader. Through your direct study responsibilities you will also contribute to the management of external stakeholder relationships by helping Roche to be the preferred sponsor for sites, patients and other important healthcare providers. • DELIVER STUDY EXECUTION by providing operational expertise into protocol design and feasibility, country selection, patient centricity and data delivery plans in partnership with cross-functional stakeholders. Ensure study quality and integrity by developing and maintaining study systems and documentation (including informed consent forms, communication plan, Trial Monitoring Plan, Trial Master File etc)., • PROVIDE COUNTRY OVERSIGHT, for insourced studies, by supporting or managing feasibility assessments to ensure countries and sites are selected for participation in studies. Provide guidance to country operational representatives during studies to ensure countries start-up on time and deliver on their recruitment commitments., • MANAGE VENDOR PERFORMANCE by providing direction and actively managing relationships. Ensure vendors and third-party suppliers deliver against contracted scope of work and performance expectations and adhere to all appropriate standards (including ICH/GCP, SOPs and other regulations)., • PLAN DEMAND AND SUPPLY by overseeing the forecasting and maintenance of supplies (including IMP) needed to ensure sites have the necessary resources to run clinical studies., • MANAGE RISK AND COMPLIANCE by assisting the study team in the identification, management and mitigation of study-related risks and issues in your areas of responsibility (including oversight of the risk, action and decision logs)., • DRIVE OPERATIONAL EXCELLENCE by providing operational expertise across a range of operations-related activities that drive improvement and consistency in the execution of clinical studies. In Clinical Operations, mindset and behaviours are as important to us as skills and capabilities. You will succeed in the contractor Study Manager role by role modelling system thinking (connecting the bigger picture), agile behaviours (working flexibly, dealing with ambiguous situations, showing resilience), empowerment and accountability (using analytical thinking, tools, good judgement, and advice-seeking to make the right decisions), a growth mindset (fostering an exchange of ideas and experimentation) and creating value (helping to connect peers' work to a collective purpose). Where pay transparency applies, details are provided based on the primary posting location. For this role, the primary location is Welwyn. If you are interested in additional locations where the role may be available, we will provide the relevant compensation details later in the hiring process. You are talented and passionate. You are inspired by our mission and would fit in well with our collaborative, patient-centric and entrepreneurial spirit. • You have Global Clinical Trial Management experience - a must have on the role, • Have a growth mindset and are excited about learning through experience, • Feel comfortable thinking on your feet and thrive in fast - paced, ambiguous and highly collaborative environments, • Hold a university degree or equivalent years of experience (preferred focus in life sciences), • Have demonstrated strong and consistent performance as a Study Manager (or equivalent) in pharmaceutical and/or healthcare industry and drug development experience (therapeutic area experience a plus), • A self-starter who finds passion in achieving successful outcomes and delivering excellence Want to make a difference and find excitement in innovating practices and challenging convention, • Possess strong working knowledge of drug development process and respective regulations, including ICH and GCP guidelines Doing now what patients need next We believe it's urgent to deliver medical solutions right now - even as we develop innovations for the future. We are passionate about transforming patients' lives. We are courageous in both decision and action. And we believe that good business means a better world. That is why we come to work each day. We commit ourselves to scientific rigour, unassailable ethics, and access to medical innovations for all. We do this today to build a better tomorrow. We are proud of who we are, what we do, and how we do it. We are many, working as one across functions, across companies, and across the world. pRED CLINICAL OPERATIONS: Our North Star is to increase R&D Productivity and Patient Inclusivity. This is supported by our CO Strategy to deliver value for pRED CO and our portfolio. We aspire to be a leading edge Clinical Operations organisation that drives innovative patient-inclusive approaches in study design and execution, utilises advanced analytics to drive data-driven decisions, and embeds innovative technologies into our ways of working to improve productivity delivery of programs and studies. We strive to create a workplace where team members own their own development and learning and are empowered to create and innovate. A healthier future drives us to innovate. Together, more than 100'000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact. Let's build a healthier future, together. The statements herein are intended to describe the general nature and level of work being performed by employees, and are not to be construed as an exhaustive list of responsibilities, duties, and skills required of personnel so classified. Furthermore, they do not establish a contract for employment and are subject to change at the discretion of Roche Products Ltd. At Roche Products we believe diversity drives innovation and we are committed to building a diverse and flexible working environment. All qualified applicants will receive consideration for employment without regard to race, religion or belief, sex, gender reassignment, sexual orientation, marriage and civil partnership, pregnancy and maternity, disability or age. We recognise the importance of flexible working and will review all applicants' requests with care. At Roche difference is valued and we are proud to be an equal opportunity employer where you are encouraged to bring your whole self to work. #J-18808-Ljbffr

Data Modeling Expert### Data Modeling ExpertApply: Welwyn: Full time: Posted Today: End Date: November 9, 2026 (13 days left to apply): 202608-120468At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.### ### The PositionA healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That’s what makes us Roche. Advances in AI, data, and computational sciences are transforming drug discovery and development. Roche’s Research and Early Development organisations at Genentech (gRED) and Pharma (pRED) have demonstrated how these technologies accelerate R&D, leveraging data and novel computational models to drive impact. Seamless data sharing and access to models across gRED and pRED are essential to maximising these opportunities. The new computational sciences Center of Excellence (CoE) is a strategic, unified group whose goal is to harness this transformative power of data and Artificial Intelligence (AI) to assist our scientists in both pRED and gRED to deliver more innovative and transformative medicines for patients worldwide.Within the CoE organisation, the Data and Digital Catalyst organisation drives the modernisation of our computational and data ecosystems and integration of digital technologies across Research and Early Development to enable our stakeholders, power data-driven science and accelerate decision-making.Join the newly formed Computational Sciences Center of Excellence (CoE) as a Data Modeling Expert, a key role within our Data Connectivity team. You will serve as a key contributor in the data modeling, semantics, ontologies, and standards space, ensuring our data are FAIR (Findable, Accessible, Interoperable, and Reusable), high-quality, and trustable; enabling scientists, computational tools, and AI algorithms from across our Research and Early Development (REDs) organizations to effectively leverage and utilize these data assets. As our Data Modeling Expert, you will: Act as a key subject matter expert on data modeling, ontologies, semantics, and standards efforts, interfacing closely with business/scientific stakeholders and informatics/engineering colleagues. Translate complex scientific requirements from various parts of R&D into clear draft data models that can be leveraged by the wider FAIR data modeling team. Independently contribute to and on occasion drive the development of data models and standards and/or information architecture solutions potentially leading function-level efforts related to FAIR data processes relating to data modeling, standards development and/or information architecture. Independently contribute to and on occasion drive strategies that ensure pan-RED Roche data is ready for AI/ML (AI data readiness), potentially leading tactical efforts around AI/data policies in partnership with other colleagues in the broader team. Independently contributes to and on occasion drive efforts that enable data quality tracking, potentially leading strategies that allow us to track and measure data quality (e.g. tracking how well annotated xRED data is). Foster a OneRoche data-centric mindset within the team, advocating for data standards, governance, and FAIR principles.* Contribute to the development, implementation and improvement of Data Governance strategies as it relates to data standards.Who You Are: You hold a Master's degree or higher in a scientific or technical field. Experienced in Data Governance, Data Standards, Data Modeling, Ontology Development, or related fields. You are proficient in one or more critical relevant scientific or data domains, and are able to provide leadership to initiatives based on that knowledge. You are an exceptional communicator with strong networking capabilities, able to build relationships and lead effectively in a matrixed organization.* You have experience working within a Research & Development organization and have a deep understanding of its processes and data handling activities.This role is based onsite at our Welwyn office.#ComputationCoE #J-18808-Ljbffr

For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. Find out more about the daily tasks, overall responsibilities, and required experience for this opportunity by scrolling down now. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.Job OverviewThe Head of Legal and Compliance, UK and EMEA will serve as the senior legal and compliance leader for Charles River Laboratories across the United Kingdom and Europe, the Middle East and Africa. Reporting to the Deputy Head of Global Business, this role will provide practical, business-oriented legal and compliance support to regional leadership, commercial and operational teams, and functional partners across a complex, highly regulated multinational environment. The role requires a UK qualified lawyer with substantial law firm and in-house experience, strong commercial and compliance judgment, and the ability to manage other legal professionals while operating effectively across jurisdictions, cultures, business units, and legal systems. This leader will be expected to balance commercial execution, regulatory expectations, ethical business conduct, enterprise risk management, and Charles River’s mission, values, and reputation. Job DescriptionEssential Duty / ResponsibilityRepresentative ActivitiesEstimated Time AllocationRegional legal leadership and business counselingServe as senior Legal and Compliance advisor for the UK and EMEA; support regional leadership, commercial and operational teams; advise on legal risk, governance, regulatory expectations, and business strategy.25%Commercial contracting and strategic business supportLead or oversee support for customer agreements, RFPs, contract negotiations, strategic collaborations, supply arrangements, partnership matters, and other regional commercial priorities.25%Compliance, ethics, and risk managementPartner with Global Compliance on program implementation, anti-bribery and anti-corruption, third-party risk, investigations, training, monitoring, controls, risk assessments, and remediation.20%People leadership and legal function managementManage, develop, mentor, and provide direction to legal professionals supporting the UK and EMEA; promote consistency, efficiency, accountability, and practical service delivery.15%Cross-functional partnership and outside counsel managementCoordinate with global Legal, Compliance, Finance, HR, Quality, Regulatory, Privacy, Trade Compliance, Procurement, and business teams; manage regional outside counsel and external advisors.10%Regional legal and regulatory monitoringMonitor legal, enforcement, market, and regulatory developments across the UK and EMEA and translate emerging requirements into practical business guidance.5%Total100%Regional Legal Leadership and Business SupportServe as the senior Legal and Compliance representative for the UK and EMEA region, providing practical, timely, and business-oriented advice to regional, commercial, operational, and functional leaders.Advise on legal issues affecting business strategy, customer relationships, commercial execution, regulatory compliance, market access, operations, and enterprise risk.Partner closely with global Legal and Compliance leaders to ensure alignment with Company standards, policies, risk tolerances, and strategic priorities.Monitor legal, regulatory, enforcement, industry, and market developments across the UK and EMEA and translate emerging requirements into practical guidance for the business.Job Description (cont.)Commercial Contracting and Strategic Business MattersLead or oversee regional commercial legal support, including customer agreements, requests for proposals, contract interpretation, negotiation strategy, escalation management, template use, and alignment with global contracting standards.Provide legal support for complex commercial initiatives, strategic collaborations, customer programs, supply arrangements, procurement-adjacent matters, and other regional business priorities.Support M&A diligence, integration, divestitures, partnerships, and other strategic transactions affecting the UK and EMEA region, coordinating with global subject matter experts as needed.Help business stakeholders achieve commercial objectives while appropriately managing legal, compliance, operational, financial, and reputational risk.Compliance, Ethics, and Risk ManagementPartner with the global Compliance function to implement, reinforce, and continuously improve Charles River’s ethics and compliance program across the UK and EMEA.Provide guidance on anti-bribery and anti-corruption, third-party risk management, government interactions, conflicts of interest, competition law, trade compliance, privacy, investigations, training, monitoring, and other business-integrity matters.Support regional compliance risk assessments, mitigation plans, controls, remediation, and reporting in coordination with global Legal, Compliance, Internal Audit, Finance, Human Resources, Quality, Regulatory Affairs, and business stakeholders.Promote a culture of integrity, accountability, responsible escalation, and ethical decision-making across the region.Team Leadership and Cross-Functional PartnershipManage, develop, mentor, and provide practical leadership to legal professionals supporting the UK and EMEA region, including direct and indirect reports as assigned.Build strong working relationships across Legal, Compliance, commercial, operational, finance, procurement, HR, quality, regulatory, privacy, trade compliance, and other functional teams.Promote consistency, efficiency, accountability, and collaboration in legal and compliance service delivery across the region, while preserving appropriate flexibility for local legal and business requirements.Manage regional outside counsel and external advisors with a focus on quality, responsiveness, business practicality, cost discipline, and alignment with Company objectives.Job QualificationsUK qualified lawyer in good standing, with authorization to practice law in the United Kingdom.At least 12 years of progressive legal experience, including meaningful experience practicing at law firms and in-house with multinational companies.Substantial commercial legal experience, including complex contracting, customer-facing business support, negotiation strategy, risk allocation, and support for commercial and operational leadership. Strong compliance experience, including anti-bribery and anti-corruption, third-party risk, investigations, training, monitoring, policy implementation, and business ethics in a multinational environment.Experience supporting government-facing matters, distributor and third-party relationships, regulatory inspections, import/export matters, data protection, privacy, employment, disputes, and internal investigations.Demonstrated experience managing, developing, and mentoring lawyers or other legal professionals.Strong understanding of legal and regulatory issues affecting multinational life sciences, pharmaceutical services, biotechnology, CRO/CDMO, research services, manufacturing, or other highly regulated global businesses.Excellent drafting, negotiation, analytical, issue-spotting, and problem-solving skills, with the ability to provide clear, practical, and business-oriented legal advice.Demonstrated ability to work effectively in a matrixed global organization and influence stakeholders across functions, geographies, cultures, and levels of seniority.High integrity, sound judgment, discretion, executive presence, and ability to manage sensitive matters independently while escalating appropriately.Preferred QualificationsPrior experience serving as a regional or country legal lead for the UK, Europe, or broader EMEA region within a U.S.-listed or other global multinational company.Experience in life sciences, pharmaceutical services, biotechnology, CRO/CDMO, research services, laboratory services, healthcare, manufacturing, or another regulated global business.Experience supporting government-facing matters, distributor and third-party relationships, regulatory inspections, import/export matters, data protection, privacy, employment, disputes, and internal investigations.Experience improving legal and compliance processes, templates, playbooks, training, intake models, contract management practices, and scalable service delivery in a regional or global legal function.Professional AttributesTrusted advisor with excellent judgment, integrity, discretion, and credibility with senior leaders.Pragmatic, proactive, and solutions-oriented lawyer who understands business objectives and provides clear, actionable guidance.Strong commercial acumen and ability to balance legal requirements, regulatory expectations, operational realities, compliance obligations, and business priorities.Collaborative, low-ego partner who builds trust across global, regional, and local teams.Clear and concise communicator who can distill complex legal and compliance issues for business and functional stakeholders.Comfortable operating in a fast-paced, global, highly regulated environment with ambiguity, competing priorities, and sensitive matters.Committed to Charles River’s mission, values, ethical standards, and reputation for scientific and operational excellence.Workplace RequirementsThe role operates in a general office or remote work environment. Occasional domestic and international travel may be required to support regional business needs, leadership meetings, investigations, transactions, and other Company priorities.Compensation DataThe hiring range for this position in the United Kingdom is 120,000/yr • 165,000/yr GBP. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, location and any collective agreements, if applicable. Remote candidates located outside the United Kingdom should be aware that the relevant pay range varies based on country and location.About Corporate FunctionsThe Corporate Functions provide operational support across Charles River in areas such as Human Resources, Finance, IT, Legal, Sales, Quality Assurance, Marketing, and Corporate Development. They partner with their colleagues across the company to develop and drive strategies and to set global standards. The functions are essential to providing a bridge between strategic vision and operational readiness, to ensure ongoing functional innovation and capability improvement. About Charles RiverCharles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of 80% of the drugs approved by the FDA in the last five years.At Charles River Laboratories, we recognize and recruit all talent. xrnqpay We are a company committed to fostering a sense of belonging and work daily in this direction.237197Job ID: 237197enUSEmployment Type: ExemptJob Area: LegalPosted Date: 29/10/2026

As a Senior Machine Learning Engineer, you will build, own, and continuously improve the scalable AI/ML systems, applications, and data infrastructure that unlock the potential of our diverse scientific data, accelerating the discovery and development of life-changing treatments. Master's or PhD in

Clearline Recruitment Ltd is assisting a global pharmaceutical client to appoint an Associate Director of Pharmacovigilance in Welwyn Garden City. This senior role provides scientific leadership across pharmacovigilance and safety science, supporting clinical development and post-marketing products within a global safety framework. The role offers hybrid working (2 days in the office), a 12-month contract outside IR35, and exposure to strategic safety initiatives within a collaborative global #J-18808-Ljbffr

Roche Welwyn is seeking a skilled software engineer to build robust scientific software solutions and scalable data pipelines supporting AI/ML use cases across drug discovery and translational medicine.You will work with scientists, data engineers and product leaders to deliver cloud-native, API-fir

We're now seeking an exceptional leader to join us as Head of Water Quality & Scientific Services; a critical role responsible for shaping our water quality strategy, leading scientific excellence, and ensuring regulatory compliance from source to tap. You'll lead a multidisciplinary team of approxi

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. The Position At Roche, our Global Product Development Safety & Risk Management (PDS) department aims to enhance healthcare for patients by elucidating and communicating the safety profile of Roche medicines to optimize their benefit-risk profile. The Opportunity The Group Director of Safety Analytics and Reporting (SAR) provides strategic leadership, expertise and oversight for safety data science, pharmacoepidemiology, analytical excellence and complex safety information reporting throughout the Roche product lifecycle. They ensure that high-quality evidence from safety databases, real-world data, and literature is generated accurately and in a timely manner. This role is a vital enabler for GxP compliance and advanced scientific safety research. As a member of the PVSD Leadership Team, the Group Director leads the global SAR function across Basel, Welwyn, and South San Francisco. This role integrates GxP safety knowledge with advanced safety data science expertise to support process experts across GVP, GCP, and medical devices safety. By partnering with PDS, R&D, and Roche Digital Technology (RDT), the Director drives the evolution of innovative evidence generation and analytical data science. The Group Director also ensures safety analysis adheres to global regulations and policies. Ultimately, the team collaborates cross-functionally to provide technical expertise and high-quality safety deliverables throughout the entire Roche asset lifecycle. The Group Director leverages the strengths of a diverse global team and creates an inspiring environment where the SAR team members feel empowered to take ownership of deliverables, build knowledge and deploy resources effectively, always striving for continuous improvement. The SAR team's remit spans four main areas: • Safety reporting: Safety database activities for regulatory deliverables and insights, • Safety data science: Advanced analytics and modeling on selected safety endpoints, including signal assessment, • Pharmacoepidemiology: Providing context for clinical/medical safety assessments, patient safety research, and regulatory reporting, • Pharmacovigilance Support: Complex literature searches for ICSR identification and signal management Primary Responsibilities and Accountabilities: • Leadership: Provides line-leadership for the global SAR sub-function; coaches members to maximize potential and well-being while sustaining a climate of purpose and urgency, • Strategic Direction: Provides vision for safety analytics, data science, pharmacoepidemiology, and literature analysis. Ensures the team executes consistent evidence generation to meet PDS obligations, • Operations & Compliance: Ensures 24/7 database access (delegated by EU QPPV) and timely, accurate execution of searches (DSURs, PBRERs, signal detection, audits). Ensures inspection readiness and timely CAPA responses, • Technical Expertise: Provides SME guidance on analytical/statistical methods and technologies (AI, LLMs, Safety AI frameworks), • Technical tools: Ensures that the SDS team has access to relevant data sources and analytics tools to perform comprehensive analysis in support of characterizing risk., • Evidence Generation: Leads PDS strategy for Real World Data/Evidence (RWD/E) to support the Roche portfolio, collaborating closely with PDD and PDMA, • Resource Management: Oversees recruitment, onboarding, and deployment of SAR resources across multiple locations based on strategic value, • Stakeholder & Strategy: Partners and maintains relationships with key stakeholders; anticipates future opportunities via internal/external networks. Contributes to PVSD leadership in scenario planning, prioritization, and budget management Who you are • You hold an advanced degree in Data Science, Quantitative/Natural Sciences, or are a qualified health professional, supported by at least 10+ years of experience in PV/safety, clinical data, or pharmacoepidemiological analysis, • You possess at least 5 years of people leadership experience and a proven track record of delivering high-quality evidence within highly regulated GxP environments and complex, high-risk projects, • You offer 5+ years of experience with drug safety databases and expert-level knowledge of the drug development lifecycle, from first-in-human trials to marketed products, • You demonstrate hands-on mastery of statistical analysis and medical data reporting, complemented by a strategic understanding of AI-based approaches like LLMs and Neural Networks, • You exhibit advanced analytical thinking and highly developed communication skills, enabling you to synthesize complex information, influence global collaborations, and drive decisions amidst ambiguity, • You utilize highly developed communication and influencing skills to build global collaborations and drive decisions, • You maintain comprehensive knowledge of data structures and business processes to guide direct reports, while being fluent in English (proficiency in German is a plus) Location & Travel Requirements • This position must be based in either Basel, Switzerland or Welwyn Garden City in the United Kingdom. Although this can be a hybrid role, with an expectation of ongoing and sustained site presence, in compliance with local company site requirements, • International business travel may be required. Typically, this will be required around 10% of the time, depending upon the site location of the jobholder and/or the requirements of the role for ongoing leadership or business project-related activities Scientific rigour and creativity, inclusive teamwork and exceptional delivery are key behaviours that drive our mission of doing now what patients need next. Together, we can be transformative. Where pay transparency applies, details are provided based on the primary posting location. For this role, the primary location is Basel. If you are interested in additional locations where the role may be available, we will provide the relevant compensation details later in the hiring process. Who we are A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact. Let’s build a healthier future, together. Roche is an Equal Opportunity Employer. #J-18808-Ljbffr

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. In Patient Safety Operations, our Safety Data Acquisition & Partnering (SDAP) team establishes the vital frameworks through which safety data enters our organisation, driving regulatory compliance and scientific insights to protect patients globally. As trusted Safety partners across Roche, we pioneer innovative safety data acquisition strategies and deliver high quality safety agreements. We thrive in a complex, evolving landscape by pragmatically solving challenges, challenging the status quo and leveraging strong cross-functional networks. In this role, you will lead clinical safety data acquisition, serving as the go‑to expert collaborating across global matrix teams to shape clinical study setups / acquisitions and safety operations. • Lead Clinical Study Safety Integration: Act as the go‑to subject matter expert to incorporate drug safety requirements directly into clinical study setups / acquisitions, data management protocols, and medical device / combination product frameworks., • Drive Process Excellence & Innovation: Design, optimise, and oversee global clinical safety data workflows- continuously challenging the status quo to establish agile, compliant, and high‑quality data intake across dynamic regulatory environments., • Oversee Performance & Quality Control: Establish KPIs, quality controls, and metrics to monitor clinical safety data flow, exercising pragmatic problem‑solving to forecast bottlenecks and maintain continuous inspection readiness., • Leverage Cross‑Functional Networks: Build and utilise strong networks across Clinical Operations, Data Management, Regulatory, Safety Risk Management, and Affiliate offices to influence stakeholders and drive end‑to‑end trial alignment., • Coach, Inspire & Present: Serve as a functional subject matter expert (SME) - coaching cross‑functional squads, representing SDAP in cross‑functional forums, and fostering a collaborative, quality‑driven culture., • Education: Degree‑level qualification in a scientific, healthcare, or related life sciences discipline., • Pharmacovigilance & Data Intake Expertise: Substantial experience in pharmacovigilance, with specialised expertise in safety data collection requirements, data intake channels, and global PV operational standards., • Clinical Trial Safety & Data Integration: Proven background in clinical study setup and clinical data management, with hands‑on experience incorporating pharmacovigilance requirements directly into clinical trial execution frameworks and data protocols., • Pragmatic Ownership & Scope: Proven ability to deal pragmatically with complex and ambiguous operational scenarios, acting as the recognised go‑to owner and subject matter expert for assigned clinical safety data deliverables., • Process Innovation & Data Workflows: Proactive drive to continuously challenge the status quo, questioning existing practices to optimise clinical data workflows and enhance data flow efficiency across the broader pharmacovigilance ecosystem., • Cross‑Functional Influence & Networking: Strong interpersonal capabilities with a demonstrated track record of building trust quickly across diverse teams and engaging cross‑functional partners to navigate complex workflows., • Subject Matter Leadership & Communication: Established SME capability with direct experience presenting complex safety data topics in cross‑functional forums and effectively representing safety acquisition requirements to internal and external operational partners., • Medical Device & Combination Products (Preferred): Experience or familiarity with medical device and combination product safety data requirements is a plus, alongside core pharmaceutical drug experience., • On‑Site & Flexible Working: Ability to work from our Welwyn Garden City site at least 51% of the time (approximately 2.5–3 days per week), balancing in‑person team collaboration with flexible remote working., • Mobility: Willingness to travel internationally as required (approximately 10–20%). Together, we’ll advance along the whole patient journey with the aspiration to prevent, stop and cure diseases. A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life‑changing healthcare solutions that make a global impact. The statements herein are intended to describe the general nature and level of work being performed by employees, and are not to be construed as an exhaustive list of responsibilities, duties, and skills required of personnel so classified. Furthermore, they do not establish a contract for employment and are subject to change at the discretion of Roche Products Ltd. At Roche Products we believe diversity drives innovation and we are committed to building a diverse and flexible working environment. All qualified applicants will receive consideration for employment without regard to race, religion or belief, sex, gender reassignment, sexual orientation, marriage and civil partnership, pregnancy and maternity, disability or age. We recognise the importance of flexible working and will review all applicants’ requests with care. At Roche difference is valued and we are proud to be an equal opportunity employer where you are encouraged to bring your whole self to work. #J-18808-Ljbffr

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. A healthier future. It's what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That's what makes us Roche. This role is based in the Real-World & Clinical Data Strategy (RWCDS) team which drives data excellence and analytics to power enhanced decision-making and evidence-generation within Roche Product Development. We develop and implement data strategies that unlock the value of clinical, operational, and real-world data to accelerate evidence generation, decision-making, and innovation across PD and beyond. By embedding FAIR principles, advancing data governance, and enabling data productization, RWCDS ensures that data is not only findable and usable, but also a driver of scientific rigor, regulatory readiness, and AI-powered transformation. Through deep partnerships with internal functions and external collaborators, we shape a future-ready data ecosystem that supports personalized healthcare and efficient drug development. The Opportunity The RWD Scientist plays a key role in generating insights from real-world data to inform clinical development, regulatory strategy, and healthcare decision-making. You will design and execute observational studies, contribute to data strategy, and collaborate across teams within Development and the broader Pharma organization. Your work enables evidence generation across therapeutic areas and supports the responsible and impactful use of real-world data at scale. • You apply in-depth knowledge of RWD and observational research to support study design, data analysis, and evidence generation across disease areas, • You solve complex data science problems using fit-for-purpose analytical tools and real-world data assets, contributing to development, regulatory, payer and other strategic deliverables, • You act as a functional resource and lead moderate-sized projects or data science activities focused on real-world data applications in clinical development, • You build proficiency in independently leading substreams or large-scale cross-functional projects focused on RWD integration into clinical development and decision-making processes, • You collaborate with cross-functional teams to define RWD needs, develop data pipelines, and ensure scientific rigor in execution and documentation, • You build expertise in novel data types, statistical methods, programming languages, and analytical methodology, which may include advanced analytics, special trial designs and types, and data handling methods, • You support knowledge sharing, tooling standardization, and continuous improvement in RWD methodology and delivery, • You continuously look for opportunities to broaden knowledge, capabilities and skill set Who you are • You hold a Master's or PhD in Epidemiology, Biostatistics, Data Science, or a related field, • You have a minimum of 5 years of experience with RWD analyses or epidemiological studies in healthcare or pharma; or an advanced degree with 3 years of equivalent work experience., • You have familiarity with RWD platforms, regulatory frameworks, and standard data models, • You have the capacity for independent thinking and ability to make decisions based upon sound principles, • You exhibit excellent strategic agility including problem-solving and critical thinking skills, and agility that extends beyond technical domain, • You demonstrate respect for cultural differences when interacting with colleagues in the global workplace, • You possess excellent verbal and written communication skills, specifically in the areas of presentation and writing, with the ability to explain complex technical concepts in clear language Preferred • Practical experience working with EMR, claims, registry, or digital health data, • Experience contributing to submissions or publications involving RWD, • Experience in the cardiovascular, renal, or metabolic disease therapeutic area is a plus, • Exposure to pharmacoepidemiology or HEOR Location • This position is based in Welwyn, UK, • Relocation Assistance is not available Where pay transparency applies, details are provided based on the primary posting location. For this role, the primary location is Welwyn. If you are interested in additional locations where the role may be available, we will provide the relevant compensation details later in the hiring process. A healthier future drives us to innovate. Together, more than 100'000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact. Let's build a healthier future, together. The statements herein are intended to describe the general nature and level of work being performed by employees, and are not to be construed as an exhaustive list of responsibilities, duties, and skills required of personnel so classified. Furthermore, they do not establish a contract for employment and are subject to change at the discretion of Roche Products Ltd. At Roche Products we believe diversity drives innovation and we are committed to building a diverse and flexible working environment. All qualified applicants will receive consideration for employment without regard to race, religion or belief, sex, gender reassignment, sexual orientation, marriage and civil partnership, pregnancy and maternity, disability or age. We recognise the importance of flexible working and will review all applicants’ requests with care. At Roche difference is valued and we are proud to be an equal opportunity employer where you are encouraged to bring your whole self to work. #J-18808-Ljbffr

Roche Welwyn is seeking a Data Modeling Expert to drive data modeling, semantics, and standards across REDs. You will translate scientific requirements into robust data models and support AI/ML readiness for data assets. The role emphasizes governance, FAIR principles, and cross-functional collaboration within the Data Connectivity team. Based onsite at Welwyn, you will influence information architecture and contribute to data quality strategies while working in a global, innovative environment #J-18808-Ljbffr

Data Steward (Master & Operational Data)### Data Steward (Master & Operational Data)Apply: Welwyn: Full time: Posted Today: End Date: November 12, 2026 (13 days left to apply): 202610-126583At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.### ### The Position The Opportunity In this role within the Real-World & Clinical Data Strategy (RWCDS) function, you will act as a pivotal bridge between technical data execution and business strategy, ensuring clinical, real-world, and operational data are accurate, accessible, and trustworthy across the Roche Product Development lifecycle. Internally known as Data Steward, you’ll be responsible for: * Drive Data Quality & Lineage: Maintain and enrich cataloging systems, data dictionaries, and metadata across key Data Domains to ensure consistency and findability in alignment with FAIR principles.* Enable Master Data Solutions: Support the operation, implementation, and ongoing maintenance of Master Data solutions and reference data across global development platforms.* Map Processes & Models: Collaborate with cross-functional partners to map data to business ways of working, contributing to conceptual data modeling and classification efforts.* Bridge Operational & Executive Stakeholders: Translate complex data governance concepts into clear, actionable insights for senior executives while working seamlessly alongside operational, scientific, and technical squads.* Ensure Compliance & Standards: Execute routine data lifecycle management, provenance tracking, and data quality checks in compliance with global data privacy and security regulations (e.g., GDPR, HIPAA).* Foster Collaborative Partnerships: Partner cross-functionally across global, multicultural teams to enhance data visibility, usability, and accessibility across the product portfolio.Who You Are You are an engaging, articulate, and thoughtful data professional who thrives on building meaningful relationships across all organisational levels. You combine technical data stewardship expertise with a mature, consultative approach to stakeholder management. * Education & Experience: Bachelor's or Master's degree in Data Science, Bioinformatics, Information Management, or Life Sciences with experience in data management or stewardship within a regulated environment.* Stakeholder Management & Presence: Exceptional communication and interpersonal skills, with demonstrated confidence in engaging both senior executive leadership and technical/operational teams.* Data Domain Expertise: Fundamental understanding of Master Data Management (MDM), reference data, conceptual data models, and FAIR data principles.* Analytical Problem-Solving: A sharp, curious mind with strong attention to detail and the maturity to navigate complex, multi-stakeholder environments with agility.* Collaborative Mindset: Proactive approach to working in cross-functional, global, and multicultural team environments. At Roche, you’ll thrive in a culture that values different perspectives and creates a place of belonging, where we challenge ourselves to excel and achieve strong results, together. ### Who we areA healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.Let’s build a healthier future, together.The statements herein are intended to describe the general nature and level of work being performed by employees, and are not to be construed as an exhaustive list of responsibilities, duties, and skills required of personnel so classified. Furthermore, they do not establish a contract for employment and are subject to change at the discretion of Roche Products Ltd. At Roche Products we believe diversity drives innovation and we are committed to building a diverse and flexible working environment. All qualified applicants will receive consideration for employment without regard to race, religion or belief, sex, gender reassignment, sexual orientation, marriage and civil partnership, pregnancy and maternity, disability or age. We recognise the importance of flexible working and will review all applicants’ requests with care. At Roche difference is valued and we are proud to be an equal opportunity employer where you are encouraged to bring your whole self to work. #J-18808-Ljbffr

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. Within Pharma Research & Early Development (pRED), our Ophthalmology teams are redefining how precision medicine can transform the detection and treatment of complex retinal diseases. This is a rare opportunity to build a new function from the ground up - establishing an Ophthalmology Precision Medicine group at our Welwyn site that brings together biomarker science, advanced imaging, clinical expertise, and artificial intelligence. You will have the platform, pipeline, and resources to shape something truly new in one of the most dynamic areas of ophthalmic research. • Build a new Ophthalmology Precision Medicine function from the ground up - defining the vision, structure, and scientific direction for a group that integrates biomarkers, advanced imaging, clinical science, and AI across the pRED Ophthalmology portfolio., • Lead a cross-functional expert team spanning translational medicine, imaging, clinical development, data science, and biomarker disciplines - ensuring precision medicine is at the heart of our Ophthalmology strategy., • Bridge laboratory science and clinical practice by steering the generation of robust fluid- and imaging biomarker strategies that enable project and disease area decisions., • Advance innovation in imaging science by directing cutting-edge ophthalmic imaging approaches including OCT, OCT-A, and FA to inform future clinical practice and therapeutic development., • Enable translational insights through AI and data by integrating preclinical and clinical datasets using classical and next-generation analytical approaches., • Influence portfolio strategy across multiple retinal diseases including neovascular AMD, diabetic macular edema, geographic atrophy, and intermediate AMD - driving the direction and future of clinical development and research., • Represent Roche externally through strong partnerships with scientific experts, investigators, and the broader ophthalmology community - remaining at the forefront of innovation., • You are a board-certified ophthalmologist (MD or MD/PhD) with deep expertise in ophthalmology, translational medicine, or biomedical sciences., • You are a recognised expert in the retina space, with a strong scientific publication record and standing as a key opinion leader in your field., • You have deep knowledge of ophthalmic imaging technologies (OCT, OCT-A, FA) and experience with imaging analysis or Reading Centre environments., • You are experienced in integrating preclinical and clinical data to support proof of biology, efficacy, and safety strategies, with some exposure to clinical trials., • You are a collaborative scientific leader who thrives in matrix environments, energised by innovation and the opportunity to build something new., • Experience applying AI or machine learning to ophthalmic imaging analysis or clinical data interpretation., • Prior experience in pharmaceutical drug development programmes for retinal diseases., • Flexible working arrangements may be available for exceptional candidates who wish to maintain some clinical activity alongside this role. A healthier future drives us to innovate. Together, more than 100,000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact. Let's build a healthier future, together. The statements herein are intended to describe the general nature and level of work being performed by employees, and are not to be construed as an exhaustive list of responsibilities, duties, and skills required of personnel so classified. Furthermore, they do not establish a contract for employment and are subject to change at the discretion of Roche Products Ltd. At Roche Products we believe diversity drives innovation and we are committed to building a diverse and flexible working environment. All qualified applicants will receive consideration for employment without regard to race, religion or belief, sex, gender reassignment, sexual orientation, marriage and civil partnership, pregnancy and maternity, disability or age. We recognise the importance of flexible working and will review all applicants' requests with care. At Roche difference is valued and we are proud to be an equal opportunity employer where you are encouraged to bring your whole self to work. #J-18808-Ljbffr

Roche in Welwyn is seeking a board-certified ophthalmologist to establish an Ophthalmology Precision Medicine group. The ideal candidate has deep expertise in ophthalmology and scientific leadership skills, with a strong publication record.

Looking for a challenging and impactful role in the biosafety field? A leading company in the biopharmaceutical industry is seeking an experienced Head of Biosafety to lead the Biosafety function fro their site in Hertfordshire. This senior position offers the chance to make a significant contribution to global pathogen safety while working in a highly regulated environment. • Provide strategic and operational leadership for the Biosafety function, ensuring its work supports organisational priorities and the wider Global Pathogen Safety strategy., • Oversee pathogen safety activities, GLP compliance, and laboratory operations within a critical and highly regulated scientific environment., • Lead, support, and develop a team of scientific professionals working across specialised biosafety and pathogen-safety activities., • Act as a senior scientific leader, applying strong pathogen-safety expertise to guide programmes, projects, and operational decision-making. To be successful in your application to this exciting role as the Head of Biosafety we are looking to identify the following on your profile and past history: • Significant professional experience working within a GLP-regulated environment., • Strong scientific expertise in pathogen safety., • Demonstrable experience leading teams within a GLP-regulated environment., • Experience supporting or leading Health Authority inspections. This role is perfect for a scientific professional with deep expertise in pathogen safety and a strong knowledge of Good Laboratory Practice (GLP). You will have the opportunity to influence the wider Global Pathogen Safety strategy and contribute directly to the safety of medicinal products used by patients around the world. Head of Biosafety / GLP / Pathogen Safety / Laboratory Operations / Scientific Leadership / Regulatory Compliance / Plasma-Derived Medicinal Products / Biopharmaceuticals / Biotechnology / CRO / Health Authority Inspections / Test Facility Management / Study Director #J-18808-Ljbffr

This job is with Boston Scientific, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. At Boston Scientific, we'll give you the opportunity to harness all that's within you by working in teams of diverse and high-performing employees, tac

Additional Locations: N/ADiversity - Innovation - Caring - Global Collaboration - Winning Spirit - High PerformanceAt Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling some of the most impor

This job is with Boston Scientific, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Boston Scientific transforms lives through innovative medical solutions that improve the health of more than 30 million patients around the world each

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A career with Boston Scientific is more than just a job. We, Boston Scientific, are an equal employment opportunity employer. So, choosing a career with Boston Scientific (NYSE: BSX) isn't just business, it's personal.

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At Boston Scientific, we'll give you the opportunity to harness all that's within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. Boston Scientific transforms lives through innovative medical technologies that improve

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In close collaboration with the national and international Medical Affairs teams, the Scientific Affairs Manager (SAM) will provide scientific and medical leadership and support for the implementation of integrated tactical and engagement plans, while upholding the highest standards of compliance an

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You will work alongside customer scientific, engineering, and IT teams to design, build, and ship integrations and data products on Tetra OS that serve scientific teams across the globe. TetraScience is the Scientific Data and AI Company building Tetra OS, the operating system for scientific intelli

As a Scientific Leader in the Discovery Integration Sciences team you will work and lead across scientific and technical disciplines in cross-functional teams designing, delivering and operating the System-of-LIAL-Systems that will power GSK’s Research activities and the underlying LIAL Platform t

Scientific Affairs Manager (SAM) for the UK & Ireland to advance medical and scientific initiatives in rare MC4R pathway diseases. You will collaborate with national and international Medical Affairs teams to deliver scientific leadership and compliant medical education across the UK. The SAM will b

Supply Chain Consultant at EPM Scientific in the DACH region and Nordics. Referrals increase your chances of interviewing at EPM Scientific by 2x.

Your work will help leaders balance cost, capacity and scientific needs, making the best use of resources to support research. Developing and implementing costing and pricing models for internal scientific services and external commercial opportunities. Shaping commercial proposals and supporting ne

UK Dementia Research Institute (UK DRI) invites a technical leader to design and build software that maps scientific questions, claims, and evidence across Alzheimer’s research. You will join as a founding member of our AI initiative, shaping Lab Brains and scientific workflows.

Thermo Fisher Scientific in Hemel Hempstead seeks an experienced Senior Manager, HPCS Marketing to shape growth across the HPCS business.

The role involves overseeing a major redevelopment programme for scientific facilities.

As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. StartYourStor y at Thermo Fisher Scienti

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You might have encountered the same problems while building search tools, scientific data systems or collaborative software. You will be a founding member of the UK DRI AI initiative, working as a peer with an engineer building Lab Brains and scientific workflows. A practical representation of scien

Thermo Fisher Scientific's Environmental and Process Monitoring (EPM) Group seeks a Senior Technical Applications Specialist to provide expert technical support and drive growth across our process monitoring portfolio.

A leading pharmaceutical company seeks a Clinical Supply Chain Manager in the UK for a full-time contract role.You will manage clinical supply chains and drive business development through strategic partnerships.Ideal candidates have experience in business development and clinical supply.This positi

This job is with Thermo Fisher Scientific, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale.

As a Medical Scientific Liaison at ViiV, you will be a trusted scientific partner to healthcare professionals across the United Kingdom. Familiarity with digital engagement tools for scientific exchange and ability to communicate through multiple channels. Scientific Relationships & Collaboration.

This job is with Thermo Fisher Scientific, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. A person with an innate scientific curiosity and keen observation skills will have the opportunity to impact the future medicine development. A

Relevant experience / knowledge in information management, scientific content or published information services in the pharmaceutical industry or a comparable scientific research environment. The Associate Director (Scientific Data and Publications) is a key role within the Research Operations & Ext

This job is with Thermo Fisher Scientific, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to acc

Our client is a fast-growing multi sector speciality distributor of chemicals and raw materials to the UK Manufacturing Industry.They are now seeking a Maintenance Engineer - Shift.This position is site based in Redditch, Worcestershire across three sites and may require working shift patterns durin