Latest regulatory affairs Jobs

Senior CMC Regulatory Strategy Manager

Leads CMC regulatory strategy for biopharmaceutical development and lifecycle management, coordinating technical submissions and ensuring compliance with global regulations. Works cross-functionally to address complex CMC issues, support inspections, and influence regulatory decisions. Focuses on maintaining product supply and optimizing regulatory processes across international markets.

GSK £144,375 – £240,625 pa

Hybrid Permanent

Senior CMC Regulatory Strategy Manager

Leads CMC regulatory strategy for biopharmaceutical development and lifecycle management, ensuring compliance with global regulations and supporting submissions, inspections, and supply continuity. Works cross-functionally to shape regulatory approaches and mentor teams, with a focus on innovation and risk mitigation in complex regulatory environments.

GSK €90,000 – €150,000 pa

Hybrid Permanent

Global Medical Affairs Director, Autoimmune Diseases

The Global Medical Affairs Director is responsible for developing and implementing strategic and operational programs for autoimmune diseases, focusing on innovative evidence, launch readiness, and post-market solutions. They lead medical-scientific input, evidence generation, and stakeholder engagement to maximize the value of new medicines and support global medical affairs initiatives.

Novartis

Hybrid Permanent

Oncology Medical Head, International

This role involves defining and executing the international medical strategy for Pfizer’s Oncology portfolio, collaborating with global and regional teams to ensure patient-centered, evidence-driven medical impact. Responsibilities include leading the scientific narrative, data interpretation, and communication across regions, as well as engaging with clinical and research leaders to drive strategic decisions and continuous improvement.

Pfizer

On-site Permanent

Oncology Medical Head, International

This senior leadership role involves defining and executing the international medical strategy for Pfizer’s Oncology portfolio, collaborating with global teams to ensure patient-centered, evidence-driven medical impact. The role requires deep oncology expertise and strong leadership to drive strategic decisions and medical execution across regions.

Pfizer

On-site Permanent

Expert Scientific Writer

This role involves leading the development of scientific publications such as manuscripts, abstracts, posters, and presentations by transforming complex clinical data into clear, accurate, and impactful content. The Expert Scientific Writer will guide materials from concept to publication, ensuring alignment with scientific narratives and industry guidelines while collaborating with cross-functional teams. The position supports global medical affairs initiatives and emphasizes high-quality, evidence-based communication across therapeutic areas.

Novartis London, United Kingdom £46,550 – £86,450 pa

Hybrid Permanent

Associate Director, Biostatistics (4)

The Associate Director (AD), Biostatistics, leads the full scope of statistical contribution to a clinicaldevelopment program. The AD provides statistical strategies for the clinical trials and regulatorysubmissions, and is accountable for the statistical deliverables within the program.Lead full scope of...

CSL

Director, Medical Evaluation & Case Processing Oversight

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...

CSL

Senior Statistician I

The Senior Statistician I will lead statistical input into clinical and preclinical study design, analysis, and reporting within AstraZeneca’s CVRM team. This role involves developing robust statistical analysis plans, applying modelling and simulation techniques, and translating complex results into actionable insights for multidisciplinary teams. The position emphasizes methodological rigor, regulatory readiness, and collaboration across global therapy areas to accelerate evidence generation for innovative medicines.

AstraZeneca Cambridge, United Kingdom

Hybrid Permanent

Sr. Research Associate, Bioanalytical & Molecular Assays - Ligand Binding Assays

This role involves developing, optimizing, and validating ligand-binding and cell-based assays to support mRNA medicine development. The candidate will generate pharmacodynamic and immunogenicity data in compliance with GcLP, using platforms like Watson LIMS and electronic lab notebooks. They will also contribute to reagent management, assay documentation, and cross-functional collaboration with clinical teams to ensure robust, regulatory-compliant data delivery.

Moderna Oxford, United Kingdom

Hybrid Permanent

Environmental Risk Assessment Scientist - 6-month Secondment

This role involves preparing and maintaining Environmental Risk Assessments, monitoring outsourced environmental studies, and engaging with cross-functional teams on sustainability initiatives. The position offers hands-on experience in regulatory science and environmental data interpretation, with full training and mentoring provided.

AstraZeneca Macclesfield, United Kingdom

Hybrid Contract Flexible

Principal Scientist, Immunogenicity and Ligand Binding Assays

This role involves leading scientific strategy and execution for immunogenicity and ligand binding assay (LBA) bioanalysis within Moderna’s mRNA-LNP therapeutic development programs. The Principal Scientist will oversee regulated assay development, validation, and sample testing, ensuring compliance with GcLP, GLP, and regulatory standards. The position emphasizes cross-functional collaboration, data interpretation, and integration of emerging technologies, including AI-enabled analytics, to support clinical decision-making across the drug development lifecycle.

Moderna

Hybrid Permanent

Head of Research and Development

We’re partnering with a market-leader in the Ophthalmology sector, who are looking to recruit an experienced Head of R&D (Research & Development)!The successful candidate will lead R&D strategy, manage a multidisciplinary team, and work closely with key internal functions to...

Evolve Selection Cambridge, Cambridgeshire, United Kingdom

Remote Permanent

Medical Devices Project Leader - Cambridge

Medical Devices Project Leader - CambridgeWe are seeking a dynamic and driven Project Leader to join our innovative medical devices team based in Cambridge. This is a unique opportunity to lead cutting-edge development projects that directly impact patient care and...

Newton Colmore Cambridge, United Kingdom

Permanent

Production Assembler (Medical Devices)

This role involves assembling electro-mechanical micro-components for sterile, active implantable medical devices in a cleanroom environment. The Production Assembler will follow strict quality and regulatory standards, maintain accurate documentation, and perform in-process inspections. It offers hands-on work in a precision manufacturing setting within a growing medtech company focused on neuromodulation.

Amber Therapuetics Oxfordshire, United Kingdom £30,000 pa

On-site Permanent