Latest regulatory affairs Jobs

Executive Regulatory Science & Strategy Director, Oncology

This role involves leading the Hematology group within Oncology Regulatory Affairs, providing strategic regulatory expertise and oversight for the development and commercialization of oncology products. Responsibilities include coaching regional and global regulatory leads, partnering with directors on innovative regulatory strategies, and representing the Global Regulatory Affairs function in senior interactions and health authority meetings.

AstraZeneca

On-site Permanent

Regional Regulatory Manager

The Regional Regulatory Manager leads the development and execution of regional regulatory strategies for assigned assets, ensuring alignment with global goals and regional requirements. This role involves close collaboration with global and local teams, providing regulatory expertise, anticipating risks, and driving timely submissions and approvals.

GSK United Kingdom

Hybrid Permanent

Regional Regulatory Manager

The Regional Regulatory Manager leads the development and execution of regional regulatory strategies for assigned assets, ensuring alignment with global strategies and regional requirements. This role involves close collaboration with global and local teams to deliver timely, compliant regulatory submissions and approvals, while providing regulatory expertise and market insights to support decision-making and risk management.

GSK

Hybrid Permanent

Head of Medical & Scientific Affairs - Respiratory & Immunology

This role involves leading the national medical strategy for respiratory and immunology therapies within the UK NHS landscape, focusing on transforming patient care pathways and accelerating access to innovative treatments. The individual will drive pre-launch and launch readiness initiatives, shape real-world evidence generation, and collaborate with cross-functional teams and external stakeholders including NICE and MHRA. Leadership of field medical teams and strategic input into regulatory, market access, and digital health initiatives are central to the position.

AstraZeneca London, United Kingdom

Hybrid Permanent

Director, Clinical Pharmacology

This role involves leading the clinical pharmacology and pharmacometrics strategy for rare disease and oncology programs, designing clinical studies, and authoring regulatory documents. You will work closely with cross-functional teams to solve drug development challenges and expedite decision-making through modeling and simulation.

Recursion United Kingdom US$212,900 – US$297,000 pa

Hybrid Permanent

Global Labelling Director, Content (Immunology)

The Global Labelling Director, Content (Immunology) will lead the development and delivery of high-quality global labelling strategies for innovative medicines. Key responsibilities include shaping labelling content, ensuring regulatory compliance, and collaborating with cross-functional teams to support successful product submissions and patient safety.

Novartis London, United Kingdom

Hybrid Permanent

Director, Clinical Pharmacology

This role involves leading the clinical pharmacology and pharmacometrics strategy for rare disease and oncology programs, designing clinical studies, and interfacing with cross-functional teams and health authorities. The position requires a Ph.D., M.D., or Pharm D. with 5-9+ years of experience in drug development, proficiency in modeling software, and strong collaboration skills.

Recursion London, United Kingdom £118,300 – £136,500 pa

Hybrid Permanent

Global Labelling Director (Team Lead), Content

This role involves leading a team of labelling professionals, developing global labelling strategies, and ensuring compliance with regulatory requirements. The Director will collaborate with cross-functional partners and drive continuous improvement in labelling processes.

Novartis London, United Kingdom

Hybrid Permanent

Executive Medical Director

Work with usOur team are passionate in the pursuit of excellence and in pushing the boundaries of cancer therapy and Autoimmune disease to deliver life-changing treatments to patients.Whilst working at Autolus you will enjoy a flexible, diverse and dynamic working...

Autolus London, W12 7RH, United Kingdom

Hybrid Permanent

Principal Scientist, Bioanalytical & Molecular Assays

This role involves leading the development and validation of advanced molecular assays such as RT-qPCR, dPCR, and NGS to support clinical biomarker strategies across Moderna’s therapeutic pipeline. The scientist will work hands-on in assay design, optimization, and data interpretation, ensuring compliance with GCLP standards while integrating genomics, bioinformatics, and clinical insights. Collaboration with cross-functional teams is key to translating molecular data into actionable decisions for drug development.

Moderna Oxford, United Kingdom

Hybrid Permanent

Global Study Lead

The Global Study Lead is responsible for managing the full lifecycle of clinical studies, from design and planning to execution and documentation. Key responsibilities include leading the study team, ensuring compliance with regulations, managing budgets, and collaborating with cross-functional teams and external partners to deliver high-quality study results.

Roche United States US$100,400 – US$186,400 pa

On-site Permanent

Global Study Lead

The Global Study Lead is responsible for overseeing the design, planning, execution, and documentation of clinical studies, ensuring compliance with regulatory requirements and delivering high-quality results within budget and timelines. The role involves leading cross-functional teams, collaborating with internal and external stakeholders, and managing study-level budgets and operational aspects.

Roche US$100,400 – US$186,400 pa

On-site Permanent

Principal Scientist, Bioanalytical & Molecular Assays

This role involves leading the development and validation of advanced molecular assays (including RT-qPCR, dPCR, and NGS) to support clinical biomarker programs across Moderna’s therapeutic pipeline. The scientist will drive end-to-end assay lifecycle management, ensure regulatory compliance with GCLP standards, and collaborate with cross-functional teams to generate high-quality genomic data for clinical decision-making. Emphasis is placed on innovation, data integrity, and integrating emerging technologies like AI-enabled tools to accelerate translational research.

Moderna

Hybrid Permanent

Senior Regulatory Associate

The Senior Regulatory Associate at Pfizer is responsible for managing regulatory activities for assigned products and markets, including new registrations, MA variations, and renewals. They will work closely with cross-functional teams, national regulatory authorities, and above-country hubs to ensure compliance and support clinical development activities.

Pfizer United Kingdom

Hybrid Permanent

Director, Medical Insights

The Director, Medical Insights role involves shaping and implementing Medical Insights processes, collaborating with various stakeholders to generate actionable insights, and embedding these insights into medical decision-making. The role focuses on advanced analytics, AI, and emerging technologies to drive value and impact across Pfizer’s medical portfolio.

Pfizer Test Valley, SO51 6HA, United Kingdom

Remote Permanent