Latest Clinical Research Associate Jobs

Clinical Development Medical Director (MD required)

The Clinical Development Medical Director is responsible for providing medical and scientific oversight for clinical trials, ensuring patient safety, and contributing to the design and execution of clinical studies. They will also participate in safety reviews, interact with healthcare professionals, and support regulatory activities.

Pfizer Marlow, United Kingdom

Clinical Development Medical Director (MD required)

The Clinical Development Medical Director is responsible for providing medical and scientific oversight for clinical trials, ensuring patient safety, and contributing to the design and execution of clinical studies. They will also participate in safety reviews, interact with healthcare professionals, and support regulatory activities.

Pfizer United States

Postdoctoral Research Associate in Fungal Genetics and Molecular Diagnostics

This role involves researching the emergence of a multidrug-resistant fungal pathogen, Trichophyton indotineae, at the intersection of genomics, antimicrobial resistance, and molecular diagnostics. You will work in a multidisciplinary team to develop new diagnostic tools and contribute to clinical and public health efforts in East London.

Queen Mary University of London London, United Kingdom £38 – £42 pa

Contract

Associate Director, Biostatistics

This role leads the statistical strategy for clinical development programs, overseeing study design, data analysis, and regulatory submissions. The individual will guide biostatistical input across trials, interact with regulatory authorities, and ensure accurate reporting of results. Collaboration with cross-functional teams and oversight of internal or outsourced programming efforts are key aspects of the position.

CSL

Hybrid Permanent

Associate Director, Biostatistics

The Associate Director, Biostatistics, leads statistical contributions to clinical development programs, including study design, data analysis, and regulatory submissions. They collaborate with cross-functional teams, manage outsourcing, and ensure the quality and timeliness of deliverables.

CSL £212,000 – £251,000 pa

Hybrid Permanent

Research Fellow in Optical Biomedical Instrumentation Development

Applications are invited for a Research Fellow in Optical Biomedical Instrumentation Development to join the Department of Medical Physics and Biomedical Engineering at University College London (UCL).The successful candidate will join the internationally renowned Biomedical Optics Research Laboratory (BORL) and...

UCL London, United Kingdom £46 – £54 pa

Contract

Clinical Development Senior Medical Director - Cardiovascular

Leads clinical development for vascular programmes across early and late phases, shaping study designs and clinical development plans. Works cross-functionally with translational science, regulatory, and commercial teams to advance medicines for vascular disease, with a focus on patient impact and scientific innovation. Provides medical oversight, contributes to regulatory submissions, and guides decision-making in a matrix environment.

GSK Stevenage, United Kingdom

Clinical Development Senior Medical Director - Cardiovascular

Lead clinical development for vascular programs across early and late-phase trials, designing studies and translational plans to advance medicines for cardiovascular disease. Collaborate with cross-functional teams to shape clinical strategies, ensure regulatory compliance, and drive patient-focused innovation within GSK’s R&D pipeline.

GSK

Vendor Program Head - Global Clinical Operations

The Vendor Program Head leads the vendor strategy and management for clinical development programs within a specific disease area. Key responsibilities include overseeing vendor execution, building high-performing teams, and ensuring alignment with development priorities and quality standards.

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

Research Assistant/ Associate in MSK Immunology & Data Science

This role involves conducting advanced bioinformatics research in the field of human tissue immunology, specifically focusing on inflammatory arthritis. You will work within a multidisciplinary team to identify new disease pathways and collaborate with specialists in the ARCADIA network.

Newcastle University Newcastle upon Tyne, Northern England, United Kingdom £33 – £46 pa

Contract

Associate Director, Clinical Supply Chain

This role involves leading end-to-end clinical supply chain strategy, managing complex global trials, and optimizing logistics and inventory management. You will work closely with cross-functional teams to ensure supply strategies align with trial milestones and commercial readiness.

Recursion United Kingdom

Associate Director, Clinical Supply Chain

This role involves leading the end-to-end clinical supply chain strategy for global trials, managing complex logistics, and optimizing workflows using AI. You will work closely with cross-functional teams to ensure supply strategies align with trial milestones and commercial readiness.

Recursion United Kingdom

Associate Director / Director, Biostatistics

This role involves providing strategic statistical leadership for Health Technology Assessment, pricing, and reimbursement activities. The candidate will work with cross-functional teams to ensure HTA evidence is scientifically rigorous and aligned with payer requirements. Responsibilities include implementing HTA methods, contributing to evidence synthesis, and mentoring biostatisticians.

Novartis London, United Kingdom

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Associate Director, Operational Intelligence

This role focuses on building advanced operational models and simulations to optimise Autolus' end-to-end processes across manufacturing, testing, supply chain, and quality. The individual will integrate data from multiple systems to create analytical frameworks that drive strategic decisions, improve capacity planning, and support business cases. It is a highly technical, insight-driven position requiring deep expertise in data modelling, cross-functional collaboration, and problem-solving in a regulated biopharmaceutical environment.

Autolus Stevenage, United Kingdom

On-site Permanent

Clinical Data & Systems Lead

This role involves leading complex clinical technology transformation and data migration initiatives across the clinical trial ecosystem. Responsibilities include managing end-to-end migration programmes, data validation, and ensuring compliance with regulatory requirements. The role also involves collaborating with global stakeholders to deliver scalable and compliant technology solutions.

HAYS Specialist Recruitment Cambridge, United Kingdom £80,000 – £120,000 pa

Hybrid Permanent