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 (non-MD)

The Global Development Lead (GDL) is responsible for leading the clinical development of assigned assets in Internal Medicine. This involves designing and executing clinical trials, creating development plans, and ensuring regulatory compliance. The role also includes collaborating with cross-functional teams, providing expert input on clinical data, and engaging with external stakeholders to drive strategic insights.

Pfizer

On-site Permanent

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

The Global Development Lead (GDL) is responsible for leading the clinical development of assigned assets in Internal Medicine. This involves designing and executing clinical trials, creating development plans, and collaborating with cross-functional teams to ensure regulatory submissions and product approvals globally. The role also includes providing expert input on trial design, regulatory activities, and engaging with external stakeholders to drive strategic insights.

Pfizer

On-site Permanent

Trial Vendor Senior Manager - Global Clinical Operations

This role involves end-to-end management of clinical trial vendors, ensuring timely and compliant delivery of services such as eCOA, central labs, and IRT. The Senior Manager leads vendor performance, financial oversight, and system validation activities while collaborating across global teams to support trial execution. Focus areas include risk mitigation, site activation, and adherence to GxP and ICH standards within a hybrid working model.

Novartis London, United Kingdom £49,140 – £91,260 pa

Hybrid Permanent

Trial Master File Oversight Manager

This role involves overseeing the quality and completeness of Trial Master Files across global clinical trials, ensuring compliance and readiness for audits. The manager will lead vendor oversight, identify documentation risks, and drive process improvements while acting as a subject matter expert. Collaboration with cross-functional teams is essential to maintain high standards in clinical documentation and support continuous innovation in TMF systems.

Novartis London, United Kingdom £49,140 – £91,260 pa

Hybrid Permanent

Executive Director, Strategy, Oncology R&D

This role involves crafting and driving the global Oncology R&D strategy, integrating clinical, scientific, and commercial insights to shape portfolio priorities. You will advise senior leadership on complex strategic decisions, optimize investment, and collaborate across functions to deliver impactful patient outcomes.

AstraZeneca Canterbury, United Kingdom

On-site Permanent

Executive Director, Strategy, Oncology R&D

This role involves owning and driving the global Oncology R&D strategy, setting priorities for the senior executive team, and transforming the approach to deliver impact for patients. The Executive Director will lead the creation of comprehensive therapeutic area strategies, provide strategic recommendations to senior leadership, and collaborate across functions to drive innovation and impact.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Senior Clinical Trial Case Manager

This role involves leading cross-functional teams in reviewing safety data, mentoring junior staff, and ensuring compliance with GxP guidelines and international regulations. The position also focuses on managing pharmacovigilance procedures, conducting impact assessments of new legislation, and supporting regulatory inspections and audits.

CSL

On-site Permanent

Senior Clinical Trial Manager

Manages clinical trial operations from start-up to closure, coordinating with CROs and internal teams to ensure timely delivery of trials in oncology and rare diseases. Focuses on process improvements and operational excellence within a fast-paced, AI-driven drug discovery environment.

Recursion London, United Kingdom £62,400 – £84,000 pa

Hybrid Permanent

Senior Clinical Project Manager

The Senior Clinical Project Manager will lead the execution of one or more clinical trials from start to finish, ensuring compliance with regulations and managing cross-functional teams. This role involves planning, budgeting, and overseeing global clinical trials, with a focus on early phase oncology studies.

Recursion United Kingdom £165,900 – £211,100 pa

Hybrid Permanent

Senior Director Global Clinical Program Lead Cardiovascular & Renal

This role involves leading the clinical development of a medicine for cardiovascular and renal conditions, managing a cross-functional team, and ensuring compliance with regulatory standards. Responsibilities include strategic planning, clinical oversight, and authoring key documents for regulatory submissions and publications.

CSL Switzerland

On-site Permanent

Sales Manager (Clinical Diagnostic Services)

This role involves driving new business and expanding customer relationships in the UK health and wellness screening market within clinical diagnostics. The candidate will lead tender processes, develop commercial opportunities, and collaborate with technical teams to deliver tailored solutions. It's ideal for someone with a scientific background looking to transition into a commercial role focused on strategic growth in a science-led environment.

VRS UK Oxford, Oxfordshire, United Kingdom £50,000 – £60,000 pa

Hybrid Permanent

(Fixed Term) Data Quality Control Specialist. Clinical Biomarker Laboratory

The Data QC Specialist will perform detailed quality control reviews of laboratory data and documentation to ensure accuracy, traceability, and compliance with regulatory standards. This role involves working closely with laboratory scientists and data management teams to resolve data discrepancies and maintain inspection readiness.

Moderna Oxford, United Kingdom

On-site Temporary

(Fixed Term) Data Quality Control Specialist. Clinical Biomarker Laboratory

The Data QC Specialist will perform detailed quality control reviews of laboratory data and documentation to ensure accuracy, traceability, and compliance with regulatory standards. This role involves working closely with laboratory scientists and data management teams to resolve discrepancies and maintain inspection readiness.

Moderna

On-site Temporary