Latest clinical research associate Jobs

Global Development Lead, Early Clinical Development, Internal Medicine

The Global Development Lead will drive clinical research for cardiometabolic diseases, creating and executing early clinical development strategies. They will work closely with cross-functional teams to translate pre-clinical observations into clinical experiments, ensuring medical and scientific excellence, and managing the delivery of clinical trial data and regulatory documents.

Pfizer Cambridge, United Kingdom

On-site Permanent

Global Development Lead, Early Clinical Development, Internal Medicine

The Global Development Lead will drive clinical research for cardiometabolic diseases, creating early clinical development strategies and leading the translation of pre-clinical observations into Phase 1/2 studies. They will work closely with cross-functional teams to ensure medical and scientific excellence, manage clinical trial execution, and engage with regulatory authorities and external collaborators.

Pfizer Sandwich, United Kingdom

On-site Permanent

Medical Director, Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead clinical research activities for GSK’s oncology portfolio, focusing on advancing the development of antibody drug conjugates (ADCs) for solid tumors. Key responsibilities include collaborating with multidisciplinary teams to design and execute clinical trials, ensuring high-quality protocol development, and engaging with key external experts to drive data generation and regulatory approvals.

GSK

Hybrid Permanent

Senior Medical Director, Oncology Clinical Development - GU

This role involves leading clinical development activities for GSK’s oncology portfolio, with a focus on genitourinary (GU) cancers. The Senior Medical Director will design and oversee phase 1–3 clinical trials, ensure scientific integrity, and collaborate with internal teams and external experts to advance drug development. The position plays a key role in regulatory submissions, lifecycle management, and shaping clinical strategy in a global, matrixed environment.

GSK Stevenage, United Kingdom US$284,250 – US$473,750 pa

Hybrid Permanent

Risk Surveillance Lead

The Risk Surveillance Lead drives the adoption of RBQM practices in clinical trials, overseeing risk assessment, documentation, and continuous improvement. They work closely with cross-functional teams to ensure quality risk management and compliance with regulatory standards.

Novartis London, United Kingdom

Hybrid Permanent

Associate Director, Translational Medicine Expert, TM Clinical Pharmacology

This role involves leading and managing multiple First-in-Human and Clinical Pharmacology studies, ensuring medical and scientific excellence. You will provide expert input into study design, safety, and reporting, and collaborate with cross-functional teams to align on program objectives and optimize processes.

Novartis London, United Kingdom

On-site Permanent

Manager, Global Regulatory Science CTA

This role involves leading the operational execution of Clinical Trial Applications (CTAs) globally, outside the US, with a focus on the UK regulatory landscape. Responsibilities include managing CTA submissions, ensuring regulatory compliance, coordinating with CROs, and leveraging advanced digital tools to enhance submission efficiency.

Moderna Poland

On-site Permanent

Manager, Global Regulatory Science CTA

This role involves leading the operational execution of Clinical Trial Applications (CTAs) globally, outside the US, with a focus on the UK regulatory landscape. Responsibilities include managing CTA activities, ensuring regulatory compliance, coordinating with CROs, and leveraging advanced digital tools to enhance submission efficiency.

Moderna

On-site Permanent

Senior Director, Head of AI for Clinical Development, Early BPRD

This role involves leading the development and application of AI in early phase clinical trials for AstraZeneca, focusing on Phase I/II programs. You will build and manage a team of AI researchers and engineers, develop reusable AI methods, and collaborate with domain experts to improve clinical trial design and decision-making.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Scientist in Translational Pathology, Oncology

This role involves working in a lab-based GCP environment, supporting translational pathology and biomarker programs. Responsibilities include maintaining quality standards, managing clinical and research specimens, performing laboratory assays, and collaborating with cross-functional teams to ensure laboratory activities align with project needs.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Research Synthesis Chemist

Your work will change lives. Including your own.The Impact You’ll MakeWe are growing our chemistry team at Recursion and are seeking a Research Synthetic Chemist to join our Automated Chemistry group. We are looking for an individual that thrives in...

Recursion Crathes, Alba / Scotland, United Kingdom

Advanced biomedical Support Worker

This role involves supporting registered Biomedical Scientists in a clinical pathology laboratory, focusing on specimen preparation, basic technical testing, and quality assurance. The worker will operate analyzers, process samples for diagnostics, maintain accurate records, and contribute to departmental quality standards. It requires precision, adherence to protocols, and the ability to work rotating shifts, including nights, within a high-pressure environment.

Acorn by Synergie Norbiton, London, KT1 3NJ, United Kingdom £13 – £16 ph

On-site Temporary

Scientific Product Manager

This role involves leading the development of scientific capabilities within an AI-driven drug discovery platform, translating complex biological challenges into product features. The candidate will act as a scientific authority, engaging with researchers and key opinion leaders, shaping product direction based on cutting-edge biology, and ensuring rigorous evaluation of AI models. They will work hands-on with agentic and LLM tools while bridging science, engineering, and commercial teams.

Owkin Paris, France

Hybrid Permanent

Senior/Principal Scientist, Ex Vivo Perfusion

This role involves leading the development and execution of human and large animal organ perfusion studies using normothermic machine perfusion (NMP) technology. The scientist will establish an ex vivo perfusion platform, generate translational data to support gene therapy programmes, and collaborate with clinical and research teams. The position requires hands-on expertise in organ handling, cannulation, and perfusion, with opportunities to mentor junior staff and influence preclinical development.

Talentmark Oxford, Oxfordshire, United Kingdom £50,000 – £75,000 pa

On-site Permanent

Procurement Manager

This role involves leading procurement activities within clinical laboratories, focusing on strategic sourcing, supplier management, and cost optimization in R&D categories. The Procurement Manager will apply specialized knowledge in genomics, bioanalytics, and related lab sciences while ensuring compliance with regulations like GCP. The position supports end-to-end delivery of procurement projects in a hybrid working environment.

Harvey Nash Welwyn Garden City, AL8 6TP, United Kingdom

Hybrid Contract