Latest clinical research associate Jobs

Medical Director, Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead the clinical research and development of GSK’s oncology portfolio, collaborating with various stakeholders to design and execute phase 1-3 clinical trials. Key responsibilities include medical oversight, protocol development, data interpretation, and engagement with key external experts to ensure the successful regulatory filing and market launch of innovative oncology treatments.

GSK

Hybrid Permanent

Medical Director, Oncology Clinical Development

The Medical Director, Oncology Clinical Development will lead clinical research activities, develop and execute oncology clinical trials, and engage with key external experts. Responsibilities include protocol development, medical monitoring, safety data review, and collaborating with various stakeholders to advance GSK’s clinical portfolio.

GSK

Hybrid Permanent

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

The Global Development Lead (GDL) is responsible for leading the clinical development of assigned assets in Internal Medicine. This involves designing, executing, and interpreting clinical studies, creating development plans, and collaborating with cross-functional teams to ensure regulatory approvals and global market access. The role also includes specialized monitoring, regulatory submissions, and engaging with external stakeholders to drive strategic insights.

Pfizer

On-site Permanent

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

The Global Development Lead (GDL) is responsible for leading the clinical development of assigned assets in Internal Medicine, working closely with cross-functional teams to design, execute, and interpret clinical studies. Key responsibilities include creating clinical development plans, regulatory submissions, and providing expert input on trial design and execution, while ensuring compliance and strategic insight generation.

Pfizer

On-site Permanent

GCP Compliance Manager (GCO)

This role involves leading quality issue management, audit coordination, and inspection readiness for global clinical trials, ensuring compliance with GCP and regulatory standards. The manager will drive self-assessments, conduct risk-based investigations, and provide expert guidance across clinical operations. It’s a high-impact compliance position requiring strong cross-functional influence and operational rigor in a hybrid working environment.

Novartis London, United Kingdom £67,900 – £126,100 pa

Hybrid Permanent

Senior Scientific Writer II

The Senior Scientific Writer II role involves developing high-quality medical and scientific communications for Novartis, including slide decks, congress materials, and advisory board content. The position requires strong collaboration with cross-functional teams to ensure content accuracy, consistency, and compliance with internal and external standards.

Novartis London, United Kingdom

Hybrid Permanent

Senior Strategy Director (Senior Consultant) – Clinical Development – Evinova

This role involves leading the development and implementation of AI and digital health strategies to transform clinical development processes. The Senior Strategy Director will act as a trusted advisor, designing digital solutions for patient recruitment, remote monitoring, and data collection while driving innovation through AI. They will lead cross-functional teams, shape operating models, and ensure digital tools are integrated into clinical protocols with a focus on measurable value and patient outcomes.

AstraZeneca Cambridge, United Kingdom

Hybrid Permanent

Associate Strategy Director (Associate Consultant) - Clinical Development

This role involves shaping AI and digital health strategies to accelerate clinical development within a collaborative, innovation-driven team. You'll work across project design, protocol development, and digital solution implementation, supporting pharmaceutical partners and AstraZeneca R&D. The position emphasizes strategic consulting, technical evaluation of digital tools, and driving value through scalable, patient-centric innovations in clinical trials.

AstraZeneca Cambridge, United Kingdom

Hybrid Permanent

Senior Project Specialist, Clinical Supplies

This role involves managing end-to-end clinical supply operations for Moderna’s mRNA-based therapies, ensuring investigational products are labeled, packaged, and distributed efficiently and in compliance with regulatory standards. The specialist coordinates with CROs, vendors, and internal teams to maintain supply chain continuity, troubleshoot logistics, and support digital innovation in supply systems, including AI-enabled tools and IRT platforms.

Moderna

Hybrid Permanent

Scientist, Clinical Biomarker Laboratory, Immuno-Assays - Cell Based

This role involves leading the development, qualification, and execution of complex cell-based immunoassays to support Moderna’s clinical trials across multiple therapeutic areas. The scientist will generate high-quality, regulatory-compliant data, serve as a subject matter expert, and collaborate with cross-functional teams and external partners. Emphasis is placed on assay innovation, scientific rigor, and integration of emerging technologies including digital and AI-enabled workflows.

Moderna

Hybrid Permanent

Vice President, Head of Clinical Operations

This role involves leading the clinical operations strategy and execution across Recursion’s development portfolio, from study planning to study closeout. You will build and mentor a high-performing team, manage global trials, and ensure operational excellence in an AI-native TechBio company.

Recursion United Kingdom

On-site Permanent

Senior Biomedical Scientist

This role involves performing routine and complex histological work with a focus on high-quality tissue dissection within an ISO 15189-accredited laboratory. You'll act as a technical reference point, ensuring best practices, supporting training, and maintaining equipment and supply continuity. The position operates in close collaboration with Consultant Pathologists within a stable, quality-driven histopathology team.

Leaders in Care Bourne, Lincolnshire, PE10 9EB, United Kingdom £45,000 – £55,000 pa

On-site Permanent

Pharmaceutical Regulatory Affairs Officer

This role involves managing regulatory submissions and product lifecycle compliance for pharmaceutical products, with a focus on packaging, labelling, and interactions with the MHRA. The candidate will coordinate eCTD submissions, support variations, and ensure change control processes are followed across cross-functional teams. It's a hands-on position offering impact in a regulated environment with hybrid working and a clear regulatory focus.

Evolve Selection Leicester, Leicestershire, United Kingdom £40,000 – £50,000 pa

Hybrid

Director Biostatistics

The Director of Biostatistics leads the statistical aspects of clinical development programs, ensuring robust study design, data analysis, and regulatory submissions. They collaborate closely with cross-functional teams and regulatory authorities to drive the success of clinical trials and therapeutic programs.

CSL

Hybrid Permanent

Director Biostatistics

The Director of Biostatistics leads the statistical aspects of clinical development programs, ensuring robust data analysis and regulatory compliance. They collaborate with cross-functional teams, manage external partners, and represent Biostatistics in regulatory interactions.

CSL

Hybrid Permanent