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Make a meaningful impact by shaping how CSL partners with clinical research sites worldwide. At CSL, we’re driven by a single purpose: to deliver innovative therapies that improve patients’ lives. The Site Engagement Group plays a key role in achieving this mission by positioning CSL as a sponsor of choice - building strong, collaborative, and sustainable partnerships with the global clinical sites that make our research possible. As an Associate Director, Site Engagement Lead, you will be the strategic bridge between CSL and our investigational sites, leading initiatives that enhance site satisfaction, strengthen collaboration, and accelerate clinical trial delivery. Key Responsibilities • Lead site engagement strategy for assigned programs or studies, ensuring sites experience seamless, coordinated interactions with CSL., • Cultivate strong, lasting relationships with key institutions, investigators, and partner sites to position CSL as a preferred sponsor., • Identify and onboard new strategic sites aligned with CSL’s pipeline and country-specific priorities., • Analyze and share site intelligence - turn data into actionable insights that inform feasibility, site selection, and recruitment strategies., • Evaluate and enhance site satisfaction, using feedback to continuously improve engagement approaches and operational processes., • Provide deep market and clinical insights into standards of care, patient pathways, healthcare systems, and regional regulatory landscapes., • Partner cross-functionally with Clinical Trial Management, Clinical Development, Site Management, Feasibility & Start-up, Medical Affairs, and other internal teams to optimize study execution and strengthen CSL’s reputation among HCPs. About You • Advanced degree in life sciences, pharmacy, or a related health field (PhD or PharmD preferred)., • 12+ years of relevant clinical research or related experience (e.g., Clinical Operations, Medical Affairs, or MSL roles)., • At least 2 years of international Clinical Trial Management experience within a sponsor or CRO environment., • Proven ability to analyze complex data, extract key insights, and present them compellingly to senior stakeholders., • Skilled in building partnerships across diverse cultures and geographies., • Strong understanding of the full drug development lifecycle and operational realities of clinical trial delivery., • Creative & strategic thinker with hands-on problem-solving ability - comfortable operating in a dynamic, fast-paced, global environment., • Influential communicator and collaborator who thrives in cross-functional settings., • High ethical standards, integrity, and a team-oriented mindset., • Willingness to travel (up to 30%, regional and international). Why Join CSL? At CSL, you’ll have the opportunity to: • Be part of a global mission-driven organization that values science, integrity, and collaboration., • Shape how CSL engages with clinical research sites, improving experiences for investigators and patients alike., • Work with passionate, experienced professionals across the globe in a culture that values innovation and continuous improvement., • Grow your impact through leadership, strategy, and data-driven decision-making in a vital area of clinical development. Join us and help make CSL the partner of choice - for sites, for investigators, and for patients everywhere. We encourage you to make your well-being a priority. It’s important and so are you. Learn more about ___ at CSL. ___ 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, ___. Our parent company, ___, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries. 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. Learn more ___

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. We are seking an Associate Director Clinical Trial Disclosure and Transparency is a global subject matter expert responsible for ensuring timely, accurate, and compliant clinical trial disclosures across all regions and study types (interventional and observational). This role guides global strategy, drives process excellence, and oversees the delivery of registration, results, and layperson summaries, anonymization and redaction of commercially confidential information (CCI) for clinical trials, in alignment with international regulations, CSL policy and industry standards and transparency requirements. Key Responsibilities Strategic Oversight & Compliance Lead enterprise clinical trial disclosure and transparency strategy and advise therapeutic areas and Medical Affairs on global requirements (e.g., FDAAA 801 and the Final Rule, clinicaltrials.gov, CTIS, EU CTR 536/2014, EMA Policy 70, Health Canada PRCI) Develop and implement scalable, efficient processes that meet evolving regulatory and industry standards Serve as the primary liaison to public registries (e.g., ClinicalTrials.gov, EudraCT, EU PAS). Disclosure Execution Oversee and deliver high-quality, compliant disclosures including study registration, protocol amendments, summary results, and lay-person summaries Ensure timely communication of disclosure obligations to clinical teams, affiliates, and stakeholders Support CROs and local teams with regional disclosure needs Transparency Execution Oversee and deliver high-quality, compliant redacted document packages for public release by global Health Authorities Advise on transparency obligations and best practices, including promotion of Smart Authoring practices, to clinical teams and functions Cross Functional Engagement Partner with Clinical Development, Biostats, Medical Writing, Regulatory, IP, Legal, Data Privacy and CMO staff to embed disclosure and transparency requirements across the development lifecycle Represent CSL’s disclosure and transparency practices internally and externally, ensuring alignment with global standards and expectations Vendor Management Select, manage, and oversee disclosure and transparency vendors to ensure high-quality deliverables and on-time execution Optimize resourcing and technology to support cost-effective delivery Metrics & Monitoring Track and report key metrics to demonstrate compliance and process performance Skills and Experience Required 10+ years in pharmaceutical/biotech environment with deep knowledge of the drug development process Expert in global clinical trial disclosure and transparency regulations, and guidelines and registries Proven track record in managing global disclosure and transparency deliverables and working in cross-functional, matrixed teams Strong understanding of ICH-GCP, ICMJE, GDPR and industry best practices Experience with vendor oversight, process improvement, and innovation in disclosure and transparency operations and transparency execution Hands on experience with the use and administration of the in Trialscope Disclose system (or equivalent) Qualifications and Education Required Bachelor’s degree in a scientific, medical, or pharmaceutical discipline required We encourage you to make your well-being a priority. It’s important and so are you. Learn more about ___ at CSL. ___ 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, ___. Our parent company, ___, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries. 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. Learn more ___

Legal Counsel, Commercial Legal Services. Reporting directly to our Associate General Counsel for Centrica Retail - Business you will have a key role in driving the realisation of Centrica's legal functions and especially the Commercial Legal Services teams objectives. Legal, Regulatory Affairs, Eth

We have a brilliant new opportunity for a Legal Counsel, Commercial Legal Services to join our Legal, Regulatory Affairs, Ethics & Compliance, and Secretariat Function (LRECS). Reporting directly to our Associate General Counsel for Centrica Retail - Business you will have a key role in driving th

A global biopharmaceutical company is seeking a Regulatory Affairs Lead to define and implement regulatory strategies for their product portfolio in the Europe Region.The ideal candidate will have extensive experience in the pharmaceutical industry, particularly in regulatory affairs, and will demon

Work with the Global Regulatory Lead and Regulatory Affairs management to define regulatory strategy and to compile and submit regulatory documents in a timely manner, leading EU HA interactions. Associate Director, Regulatory Affairs. Develop detailed regulatory project plans and support regulatory

Senior International Consultant - Regulatory Affairs and Executive search. This position supports and coordinates regulatory activities for both specialty and generic pharmaceutical products across Europe. Strong, clear evidenced experience with European regulatory frameworks and submission pathways

Line management of team of Senior Regulatory / Regulatory Affairs managers. Primary RA interface with Europe Market Access and Medical Affairs for early touch points and represent RA in Area Brand Team (ABT) as applicable to provide strategic input for regulatory approval, ensure the business needs

The Regulatory Affairs Analyst and Competition Policy Analyst is an exciting role in the Legal and Corporate Affairs (LAC) team providing senior level advice relating to antitrust, litigation, regulation, and M&A. We’re looking for a Regulatory Affairs Analyst and a Competition Policy Anal

Job Title: Regulatory Affairs Training Manager – Regulatory Information Management (RIM).

Job Title: Quality Assurance and Regulatory Affairs Specialist Location: Corsham, Wiltshire Hours of Work: Monday to Friday, 8. Are you passionate about quality, compliance, and making a real impact in the medical device industry? We're looking for a Quality Assurance and Regulatory Affai

The Regulatory Affairs (RA) Associate in the Global RA Coordination team is responsible for managing the Global RA inbox, coding invoices, reporting sales figures, archiving, and providing general support to the RA group.

All potential candidates should read through the following details of this job with care before making an application.Thanks for checking out our vacancy, we're delighted you want to learn more about Dechra!.Dechra are a growing, global specialist within the world of veterinary pharmaceuticals.Our e

Job Title: Regulatory Affairs Training Manager – Regulatory Information Management (RIM).

A leading pharmaceutical company is seeking a Head of External Partnerships to oversee global strategic partnerships within Regulatory Affairs. The ideal candidate should have significant experience in Regulatory Affairs and vendor management, along with exemplary negotiation and leadership skills.

Job Title: Regulatory Affairs Training Manager – Regulatory Information Management (RIM).

A global e-commerce leader in London is seeking a motivated Legal Counsel to provide legal guidance on regulatory compliance and consumer product safety regulations. The ideal candidate will support various teams, manage risks, and navigate the changing regulatory landscape.

Global Associate Director, Regulatory Affairs. Serves as regulatory representative to marketing or research project teams and government regulatory agencies. Drive global Regulatory Affairs strategies for the portfolio, including managing internal and external stakeholders.

Regulatory Affairs: Support engagement with regulatory authorities, including the UK’s Office for Product Safety and Standards (OPSS) and EU market surveillance authorities. Legal Counsel - Regulatory and Government Affairs. Legal Counsel - Regulatory and Government Affairs.

We are looking for an experienced and proactive Global Regulatory Affairs Associate Director Cardio‑Metabolic to join our Global Regulatory Affairs team. Global Regulatory Affairs Associate Director (Cardio-Metabolic). Significant experience in regulatory affairs within the pharmaceutical industry

A leading biotechnology firm based in Greater London is seeking a Regulatory Affairs Manager for a 12-month contract. The role involves advising on regulatory strategy, collaborating with regional stakeholders, and managing interactions with regulatory agencies. The ideal candidate will have experti

Line management of team of Senior Regulatory / Regulatory Affairs managers. Primary RA interface with Europe Market Access and Medical Affairs for early touch points and represent RA in Area Brand Team (ABT) as applicable to provide strategic input for regulatory approval, ensure the business needs

Perrigo is seeking a dynamic and experienced Regulatory Affairs Manager to lead regulatory strategy and execution for our biocidal product portfolio across multiple territories. Ensure regulatory compliance across all relevant markets and proactively manage regulatory risks. Manage and mentor the Bi

The ideal candidate will support various teams, manage risks, and navigate the changing regulatory landscape. A global e-commerce leader in London is seeking a motivated Legal Counsel to provide legal guidance on regulatory compliance and consumer product safety regulations.

A leading pharmaceutical company in the United Kingdom is seeking a Mid-Senior level Regulatory Affairs Specialist to provide regulatory input and support for new Marketing Authorisation Applications. The ideal candidate will have a strong background in regulatory submissions and CMC, with an emphas

Crucial to your success will be your ability to work closely with the FDA and other regulatory bodies to agree innovative scientific approaches and provide the internal leadership to convert this into a regulatory strategy to be followed and implemented. Vice President Scientific Affairs and Regulat

The Regulatory Affairs Analyst and Competition Policy Analyst is an exciting role in the Legal and Corporate Affairs (LAC) team providing senior level advice relating to antitrust, litigation, regulation, and M&A. We’re looking for a Regulatory Affairs Analyst and a Competition Policy Analyst in L

A prominent pharmaceutical company in the United Kingdom seeks a Regulatory Affairs Specialist to provide full regulatory support for products. The ideal candidate will have significant experience across the product lifecycle, particularly with CMC regulatory submissions.

Regulatory Affairs Manager page is loaded. Determining and/or validating existing regulatory information including legal ingredient declarations, allergen information, nutritional, analytical tolerances, suitability based on product composition in our online formulation repositories. Preventing any

We are seeking an experienced Regulatory Affairs professional to lead our medical devices and combination products clinical trial regulatory strategy. In this pivotal role, you will provide expert guidance on regulatory pathways for clinical investigations and serve as the key regulatory representat

As Head of Regulatory Affairs for the UK and Ireland, you will play a pivotal role on the Leadership Team, shaping and executing bold, forward-looking regulatory strategies across the entire pharmaceutical portfolio. Several years of experience in leading international and cross‑functional project

Recently a new vacancy has opened regulatory specialist to act as the main UK point of contact for regulatory activities. Get notified about new Regulatory Affairs Officer jobs in. Chemical Regulatory Affairs Officer.

We are seeking an experienced Senior Regulatory Manager with strong expertise in EMA regulatory affairs to join their dynamic team. Strong regulatory affairs experience with a focus on EMA submissions. This role offers the opportunity to lead regulatory strategy, manage submissions, and act as a key

Act as global regulatory affairs CMC lead for the assigned development and/or commercial products and/or projects and define and execute the Global Regulatory CMC strategy from pre‑clinical stage up to Marketing Authorisation and/or life cycle maintenance. More than 9 years professional working ex

A leading cryptocurrency firm is seeking a Regulatory Affairs Specialist to lead regulatory efforts in the UK. This role requires a minimum of 5 years of experience in regulatory or governmental affairs, excellent communication skills, and the ability to manage relationships with various stakeholder

A global biopharmaceutical company is seeking a Regulatory Affairs Lead to define and implement regulatory strategies for their product portfolio in the Europe Region. The ideal candidate will have extensive experience in the pharmaceutical industry, particularly in regulatory affairs, and will demo

Track and ensure regulatory compliance obligations such as reporting requirements into regulators are met in a timely manner, and support teams on the development, maintenance, and documentation of regulatory reporting requirements. Assistant Counsel or Specialist, Government, Policy and Regulatory

We are looking for an experienced and proactive Global Regulatory Affairs Associate Director Cardio‑Metabolic to join our Global Regulatory Affairs team. Global Regulatory Affairs Associate Director (Cardio-Metabolic). Significant experience in regulatory affairs within the pharmaceutical industry

Under general supervision participates in core regulatory activities to ensure effective regional agency interactions consistent with the Global Regulatory strategy includes contingency regulatory planning / risk assessment. Regulatory Affairs Manager - Greater London - Life Science - 12-Month Contr

The WEP Clinical Senior Regulatory Affairs Manager plays a critical role in shaping and delivering regulatory strategies across a diverse portfolio of projects, including Post-Approval Named Patient Programmes, Expanded Access Programmes, Compassionate Use Programmes, and Clinical Trials. Lead, ment

This remote position requires 3–5+ years of experience in regulatory affairs and a Bachelor's degree. A leading life sciences firm is seeking a Director, RIMS Strategy Consultant to oversee regulatory operations and manage client solutions.

Job Title: Regulatory Affairs Training Manager.

Position: Senior Manager, Global Regulatory Affairs. Represent Regulatory Affairs on cross‑functional teams and liaise with health authorities. Represent regional Regulatory Affairs or serve as Regional Lead on cross‑functional teams (e.

Regulatory Affairs Training Manager.

The RA Quality & Compliance Excellence function, part of RA Business Operations, collaborates across Global Regulatory Affairs (GRA) to ensure that regulatory processes and practices adhere to the highest standards of quality, compliance, and operational efficiency. Senior Manager, Regulatory Affair

The Regulatory Affairs team are the owners of PIC’s regulatory strategy including being responsible for managing the relationships with the relevant UK regulators (PRA and FCA). To work with the Head of Regulatory Affairs to provide papers to Management, Board Risk Committee, Audit Committee and B

Regulatory Affairs: Support engagement with regulatory authorities, including the UK’s Office for Product Safety and Standards (OPSS) and EU market surveillance authorities. Legal Counsel - Regulatory and Government Affairs. Legal Counsel - Regulatory and Government Affairs.

As an Senior Manager, Global Regulatory Affairs, Precision Medicine, you will help develop and execute Precision Medicine regulatory strategy in alignment with the drug global regulatory strategy and in compliance with the appropriate IVD regulations. Represent Regulatory Affairs Precision Medicine