Jobs in Exeter

Executive Director, External Strategy & Science Advocacy

This role involves leading the external engagement and policy advocacy for GSK's Development Sciences, working closely with regulatory agencies, industry consortia, and government bodies to shape the future of pharmaceutical innovation. The Executive Director will drive strategic partnerships, develop policy frameworks, and champion technical advancements in clinical development and data science.

GSK

On-site Permanent

Executive Director, External Strategy & Science Advocacy

This role involves leading the external engagement and policy advocacy for GSK's Development Sciences, working closely with regulatory agencies, industry consortia, and academic institutions to shape the future of pharmaceutical innovation. Key responsibilities include developing policy strategies, advancing technical capabilities, and fostering strategic partnerships.

GSK

On-site Permanent

Global Development Lead, Internal Medicine, Sr. Director (non-MD)

The Global Development Lead (GDL) is responsible for leading the clinical development of internal medicine assets, working with cross-functional teams to design and execute clinical trials. Key responsibilities include creating clinical development plans, ensuring regulatory compliance, and collaborating with external partners to advance Pfizer's clinical programs.

Pfizer

On-site Permanent

Global Development Lead, Internal Medicine, Sr. Director (non-MD)

The Global Development Lead (GDL) in Internal Medicine is responsible for leading the clinical development of assigned assets, collaborating with cross-functional teams to design and execute clinical trials, and ensuring regulatory compliance. The role involves creating clinical development plans, providing expert input on trial design and execution, and engaging with external stakeholders to drive strategic insights and support regulatory submissions.

Pfizer

On-site Permanent

Senior Clinical Trial Case Manager

This role involves leading cross-functional teams in reviewing safety data, mentoring junior staff, and ensuring compliance with GxP guidelines and international regulations. The position also focuses on managing pharmacovigilance procedures, conducting impact assessments of new legislation, and supporting regulatory inspections and audits.

CSL

On-site Permanent

Associate Director, Biostatistics (2)

The Associate Director, Biostatistics, leads the statistical contribution to clinical development programs, ensuring appropriate methodologies for study design, data analysis, and regulatory submissions. They collaborate with cross-functional teams, manage outsourcing operations, and represent Biostatistics in regulatory interactions.

CSL United Kingdom

On-site Permanent

Director – Process Design and Optimisation in Chemical Development

This role involves leading a team in the design and optimisation of chemical processes for drug development. Responsibilities include technical direction, project delivery, regulatory submissions, and mentoring scientists. The position leverages innovative technologies and AI to enhance process efficiency and ensure robust commercial processes.

AstraZeneca Macclesfield, United Kingdom

Hybrid Permanent

Director, Immunotoxicology, Immune Safety

This role involves leading the immunotoxicology strategy across AstraZeneca's BioPharma and Oncology portfolios, guiding the design and execution of experimental strategies to assess and mitigate immune-related toxicities. You will collaborate with multidisciplinary teams, influence project direction, and build a high-performing team in a highly collaborative and innovative environment.

AstraZeneca Cambridge, United Kingdom

Hybrid Permanent

Manager, Computational Biology (Early Oncology)

This role involves leading a team of computational biologists to identify and advance novel oncology therapeutics. Responsibilities include mentoring team members, driving target discovery, defining patient population strategies, and collaborating with cross-functional teams to integrate and analyze complex biological data.

Recursion United Kingdom

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

Hybrid Permanent

(Fixed Term) Analyst, Quality Control, Chemistry & Stability

The Role:Joining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients.Moderna is establishing a leading research, development, and manufacturing facility at...

Moderna Gargrave, BD23 3RZ, United Kingdom

Head of Computational Drug Design, Cambridge, MA

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 Cambridge, United Kingdom

Medicinal Drug Design 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

(Fixed Term) Analyst, Quality Control, Microbiology

The Role:Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology, with a diverse pipeline of development programs across various diseases.As an employee, you'll be part of a continually growing organization,...

Moderna Oxford, United Kingdom

Clinical Project Manager

As a Clinical Project Manager, you will manage clinical trial packaging and distribution projects from start to finish, acting as the main point of contact for clients and coordinating cross-functional teams. You will ensure projects meet timelines, budgets, and quality standards while maintaining compliance with GMP/GDP requirements and client processes.

Yolk Recruitment Blackwood, Cymru / Wales, United Kingdom £45,000 pa

Hybrid Permanent