Latest clinical research associate Jobs

Clinical Development Medical Director (Associate Director)

This role involves overseeing the medical and scientific aspects of clinical trials in Internal Medicine, ensuring data integrity and quality. Responsibilities include medical monitoring, safety data review, protocol development, and collaboration with internal and external stakeholders.

Pfizer

On-site Permanent

Clinical Development Medical Director (Associate Director)

This role involves overseeing the medical and scientific aspects of clinical trials in Internal Medicine, ensuring data integrity and quality. Responsibilities include medical monitoring, safety data review, protocol development, and providing clinical support to the study team and investigators.

Pfizer

On-site Permanent

Associate Director, Clinical Operations, Pricing and Analytics

The Role:Reporting to the Director, Business Analytics & Operations Management, the Associate Director, Business Analytics & Insights, Clinical Operations will be accountable for development and implementation of analytical & financial systems & tools and processes to perform business analytics within...

Moderna Oxford, United Kingdom

Associate Director, Clinical Operations, Pricing and Analytics

The Role:Reporting to the Director, Business Analytics & Operations Management, the Associate Director, Business Analytics & Insights, Clinical Operations will be accountable for development and implementation of analytical & financial systems & tools and processes to perform business analytics within...

Moderna

Medical Director - Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead the design and execution of phase 1-3 clinical trials for hematological malignancies. This role involves collaborating with a multi-disciplinary team to ensure patient safety, scientific integrity, and regulatory compliance, while contributing to the strategic development of GSK's oncology portfolio.

GSK

Hybrid Permanent

Medical Director - Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead the design and execution of clinical trials for GSK's oncology portfolio, focusing on hematological malignancies. Key responsibilities include collaborating with multidisciplinary teams, ensuring patient safety, and contributing to regulatory submissions and publications.

GSK

Hybrid 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

Director, Therapeutic Area Biomarker Lead (Neuroscience)

This role involves leading the development and implementation of biomarker strategies for neuroscience drug programs, integrating translational data science, and guiding cross-functional teams through clinical and regulatory processes. The Director will oversee biomarker components in clinical studies, mentor specialists, and ensure regulatory compliance while advancing precision medicine in a collaborative, innovation-driven environment.

Novartis London, United Kingdom £83,510 – £155,090 pa

Hybrid Permanent

Director, Alliance Management

This role involves leading strategic partnerships with CROs, ensuring governance, performance, and relationship management. The Director will collaborate globally, drive continuous improvement, and support cross-functional teams at AstraZeneca's Cambridge Biomedical Campus.

AstraZeneca Cambridge, United Kingdom

Hybrid Permanent

Director, CMC Regulatory Affairs

Lead the development and execution of global CMC regulatory strategies for small molecule drugs in clinical trials and marketing applications. Author and manage high-quality regulatory submissions across the US, EU, and rest of world, while advising cross-functional teams on compliance, risk mitigation, and evolving GMP standards. Collaborate closely with internal and external stakeholders to ensure timely delivery of regulatory deliverables and support clinical development programs.

Recursion London, W1C 2QP, United Kingdom

Remote Permanent

Feasibility and Recruitment Lead

This role involves leading UK feasibility and recruitment for cutting-edge cell therapy studies, translating scientific insights into actionable plans. Responsibilities include guiding end-to-end feasibility, collaborating with global stakeholders, and developing recruitment strategies to ensure timely and effective patient access to trials.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Clinical Evaluation Specialist

This role involves conducting clinical evaluations with a focus on radiology and medical imaging technologies such as CT, PET, and fluoroscopy. The specialist will leverage clinical research experience, including participation in trials and publication of research papers, to support regulatory and consultancy projects. The position is based in London with a hybrid working arrangement.

Computer Futures London, City And County Of the City Of London, United Kingdom £75,000 – £90,000 pa

Hybrid Permanent

Senior Research Investigator (In-vitro / Cellular Pharmacology), London

This role involves designing and implementing biological screening cascades for drug discovery programs, with a focus on in-vitro and cellular pharmacology. The candidate will work cross-functionally with AI and drug design teams to generate high-quality biological data, support decision-making, and advance projects from early discovery to clinical development. Emphasis is placed on mechanistic understanding of drug-target interactions in oncology, immunology, and partnered portfolios.

Isomorphic Labs London, United Kingdom

Hybrid Permanent

Team / Research Leader (Translational Oncology), London

This role involves leading the development and execution of comprehensive translational strategies for Isomorphic Labs' oncology pipeline. You will collaborate with interdisciplinary teams, manage a group of biologists, and ensure the successful transition of AI-designed drugs from preclinical to clinical stages.

Isomorphic Labs United Kingdom

Hybrid Permanent

Research Scientist, Immunology

This role involves designing and executing complex in vitro assays using primary human immune cells and patient-derived tissues to support drug discovery in immunology. The scientist will contribute to target validation, mechanism of action studies, and small molecule screening, leveraging advanced technologies like flow cytometry and high-content imaging. Working within cross-functional teams, they will integrate immunology expertise into both in vitro and in vivo workstreams across the therapeutic pipeline.

Recursion Crathes, Alba / Scotland, United Kingdom £52,000 – £70,400 pa

On-site Permanent