Latest regulatory affairs Jobs

Quality Manager (Manufacturing)

This role involves leading quality assurance and compliance across a manufacturing site in Winterbourne, ensuring adherence to ISO, GMP, and customer-specific standards. The Quality Manager will drive continuous improvement, oversee audits and CAPA, manage customer complaints, and lead a team of quality professionals. The position requires strong technical knowledge in regulated manufacturing environments and cross-functional collaboration to improve product quality and operational performance.

Rise Technical Recruitment Bristol, Bristol (county), United Kingdom £50,000 – £60,000 pa

On-site Permanent

Global Development Lead, Early Clinical Development, Internal Medicine

The Global Development Lead will drive clinical research for cardiometabolic diseases, creating early clinical development strategies and leading the execution of research projects. They will translate pre-clinical observations into clinical experiments, manage clinical trial data, and collaborate with cross-functional teams to ensure medical and scientific excellence.

Pfizer United Kingdom

On-site Permanent

Global Development Lead, Early Clinical Development, Internal Medicine

The Global Development Lead will drive clinical research for cardiometabolic diseases, creating and executing early clinical development strategies. They will work closely with cross-functional teams to translate pre-clinical observations into clinical experiments, ensuring medical and scientific excellence in Phase 1/2 studies and regulatory submissions.

Pfizer London, SW7 2AP, United Kingdom

Hybrid Permanent

Portfolio Innovation Director - Global Clinical Operations

Leads innovation in global clinical operations by identifying and integrating AI-driven and technology-enabled solutions into clinical trials. Focuses on improving trial design, patient access, and operational efficiency while working across cross-functional teams to scale impactful innovations. Requires deep clinical and drug development expertise to evaluate and implement transformative solutions.

Novartis Ireland

Hybrid Permanent

VMG Access Technology & Operations Lead

This role involves leading the advancement of AI, digital tools, and operational capabilities across VMG Access at Pfizer. Responsibilities include driving technology strategy, implementing AI and automation, shaping GTCS-related changes, enabling data-driven decision-making, and ensuring compliance and risk management.

Pfizer Spain

On-site Permanent Flexible

VMG Access Technology & Operations Lead

This role involves leading the advancement of AI, digital tools, and operational capabilities across VMG Access at Pfizer. Key responsibilities include driving technology strategy, leading AI and automation initiatives, shaping GTCS-related technology changes, and enabling data-driven decision-making to support strategic and operational insights.

Pfizer London, SW7 2AP, United Kingdom

Hybrid Permanent

Investigator Contracts Lead, Sr. Manager

This role leads the negotiation and execution of clinical trial contracts with investigator sites globally, managing both contractual terms and site budgets. The Senior Manager oversees complex or high-priority studies, resolves escalations, and collaborates with Legal, Finance, and pCRO partners to ensure timely site activation. It involves shaping contracting strategies, mentoring junior staff, and driving process improvements in a remote, global environment.

Pfizer Poland

Remote Permanent

Global Program Safety Team Lead

This role involves leading the Medical Safety organization for Novartis' Neuroscience division, managing safety strategies, and influencing high-stakes decisions. Responsibilities include managing disease areas, enhancing team expertise, and ensuring robust safety evaluations throughout the product lifecycle.

Novartis United Kingdom

Hybrid Permanent

GCP Compliance Manager - Clinical Programs & Trials

This role involves providing compliance oversight for clinical programs and trials, ensuring adherence to Good Clinical Practice standards. You will act as a primary compliance partner to Clinical Trial Teams, enabling decision-making on complex regulatory scenarios and leading cross-functional discussions to resolve quality issues.

Novartis Ireland

Hybrid Permanent

Senior Principal Developer

This role involves developing and maintaining R packages and Shiny applications to support clinical trial data analysis, automation, and reporting workflows. The developer will collaborate with statisticians and clinical teams to deliver efficient, reproducible tools, while promoting best practices in data science and software development. A strong focus is placed on responsible AI integration, open-source collaboration, and modernizing clinical reporting through user-centric design and tooling.

Novartis London, United Kingdom £57,050 – £105,950 pa

Hybrid Permanent

Clinical Development Medical Director (Associate Director)

This role involves overseeing medical and scientific aspects of clinical trials in Internal Medicine, including medical monitoring, safety data review, and clinical data management. The Medical Director will also contribute to protocol design, site selection, and investigator training, while mentoring others and ensuring data integrity and quality.

Pfizer Manchester, M1 4HD, United Kingdom

On-site Permanent

Senior QC Analyst

This role involves leading analytical testing and quality control activities for raw materials, intermediates, and finished pharmaceutical products in a GMP-regulated laboratory. The Senior QC Analyst ensures data integrity under ALCOA+ principles, supervises team members, investigates deviations and OOS/OOT results, and supports continuous improvement and compliance. It is a hands-on position with leadership responsibilities in a quality-focused scientific environment.

Smart4Sciences Almere Stad, Netherlands £10,000 – £11,000 pa

On-site Permanent

PKPD Modelling Lead, London

Isomorphic Labs is applying frontier AI to help unlock deeper scientific insights, faster breakthroughs, and life-changing medicines with an ambition to solve all disease.The future is coming. A future enabled and enriched by the incredible power of machine learning. A...

Isomorphic Labs London, United Kingdom

Safety Process Director / Senior Safety Process Director

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...

Roche Welwyn Hatfield, United Kingdom

GCP Compliance Manager - Clinical Programs & Trials

This role involves providing expert Good Clinical Practice (GCP) compliance guidance to clinical trial teams, supporting decision-making on complex regulatory issues, and ensuring adherence to quality standards across global clinical programs. The manager will lead investigations into quality issues, drive inspection readiness, and translate regulatory requirements into practical actions. Collaboration with cross-functional stakeholders is central to strengthening compliance and fostering a culture of data integrity and accountability.

Novartis London, United Kingdom

Hybrid Permanent