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

Medical Director, Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead clinical research activities for GSK’s oncology antibody drug conjugate (ADC) portfolio, focusing on advancing the development of clinical trials from early to late stages. Key responsibilities include protocol development, medical monitoring, safety data review, and collaboration with a multi-disciplinary team of experts to ensure the scientific integrity and timely delivery of clinical trials.

GSK

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

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

Principal Data Strategy & Analytics Specialist

This role involves shaping data strategies and leading advanced analytics to support evidence generation and clinical decision-making using real-world and clinical trial data. The specialist will design analytical frameworks, drive data standardization, and collaborate with global teams to integrate complex data sources for patient impact.

Roche Welwyn Hatfield, United Kingdom

Hybrid Permanent

Senior Data Strategy & Analytics Specialist

This role involves designing and executing data strategies that integrate clinical, operational, and real-world data to support drug development. The specialist will act as a subject matter expert in data curation and analytics, working closely with scientific teams to improve data accessibility and usability. The position emphasizes the application of FAIR data principles and production-grade analytical workflows within a regulated environment.

Roche Welwyn Hatfield, United Kingdom

Hybrid Permanent

Specialist Biomedical Scientist

This role involves managing and developing pathology laboratory services, including analysing specimens, supporting research, and ensuring efficient operations in blood transfusion, haematology, or chemical pathology. The scientist will work closely with consultants and managers, handle sensitive information, and participate in on-call duties with a requirement to live within 30 minutes of the hospital. Rotational shifts including early, late, weekend, and on-call hours are integral to the position.

Spire Healthcare Southampton, Hampshire, SO19 8NJ, United Kingdom

On-site Contract

Field Service Engineer, Laboratory Automation Systems

This role involves installing, servicing, repairing, and calibrating advanced laboratory automation and diagnostics systems used in NHS and clinical laboratories. The engineer will work on complex electro-mechanical and electronic systems, including flow cytometry and cell separation equipment, at customer sites. The position requires strong technical problem-solving skills and a customer-focused approach in high-pressure environments.

TRS Consulting Bowers Gifford, Essex, SS13 2HX, United Kingdom £52,000 pa

On-site Permanent