Latest clinical research associate Jobs

NIS P&D Project Management, Associate Director

The NIS P&D Project Management, Associate Director is responsible for developing and delivering high-quality Non-Interventional Studies (NIS) project plans, managing resources, and collaborating with various functional teams. Key responsibilities include maintaining accurate project schedules, driving cost and resource forecasts, and ensuring alignment with strategic goals.

GSK

Hybrid Permanent

ViiV Healthcare (GSK) Senior Director, Clinical Development

As a Senior Medical Director at ViiV Healthcare, you will lead the design and delivery of early development plans for HIV treatments, ensuring clinical excellence and medical governance across Phase 1-4 studies. You will collaborate with internal and external stakeholders to design, execute, and interpret clinical studies, focusing on long-acting medicines and ensuring patient safety and data integrity.

GSK United States

On-site Permanent

Clinical Development Scientist, Manager

The Clinical Development Scientist (Manager) role involves providing scientific oversight and support for clinical trials in Internal Medicine. Responsibilities include protocol development, data review, safety monitoring, and contributing to clinical documents and reports. The role also involves collaborating with various stakeholders, including investigators, regulatory bodies, and safety review teams.

Pfizer

On-site Permanent

Oncology Medical Head, International

This role involves defining and executing the international medical strategy for Pfizer’s Oncology portfolio, collaborating with global and regional teams to ensure patient-centered, evidence-driven medical impact. The position requires deep oncology expertise and leadership to drive strategic decisions, data interpretation, and communication across international markets.

Pfizer United States

On-site Permanent

Global Medical Affairs Director, Immunology, Rap-cel (CAR-T)

Lead the global medical strategy for a novel CAR-T therapy in autoimmune diseases, driving evidence generation, scientific engagement, and medical governance. Collaborate with KOLs, cross-functional teams, and global stakeholders to shape treatment paradigms and support lifecycle management. Serve as a scientific expert in cell and gene therapies within a high-impact, innovation-driven environment.

Novartis London, United Kingdom £93,870 – £174,330 pa

Hybrid Permanent

Senior Director, Epidemiologist

This role involves leading global epidemiology strategy for oncology programs across the drug development lifecycle, with a focus on generating real-world evidence and informing benefit-risk decisions. The Senior Director will represent epidemiology in regulatory discussions, mentor junior staff, and drive innovation in safety science methodologies. Work is conducted in a hybrid or remote setup depending on location.

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

Hybrid Permanent

Director, Statistical Programming

This role involves leading and developing a team of programmers, providing strategic direction for statistical programming in clinical development, and ensuring quality, compliance, and continuous improvement. The Director will partner cross-functionally to drive business impact and maintain industry and regulatory knowledge.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Executive Medical Director, Clinical Development Lead - Oncology - Lung & Head/Neck Cancers

This role leads clinical strategy and scientific vision for oncology assets focused on lung and head/neck cancers, shaping end-to-end development from discovery to approval. The Executive Medical Director drives integrated decision-making across regulatory, commercial, and clinical domains, leveraging advanced analytics and AI to accelerate impactful therapies. They serve as a key governance leader and external representative, ensuring strategic alignment across functions and stakeholders.

GSK

Hybrid Permanent

Principal Programmer / Analyst

The Principal Programmer / Analyst role involves leading programming activities for complex clinical studies, ensuring high-quality and timely outputs. You will collaborate with cross-functional teams, mentor junior programmers, and support regulatory interactions, while fostering innovation and quality assurance in a global, agile environment.

GSK Stevenage, United Kingdom

Hybrid Permanent

Principal Programmer / Analyst

This role involves leading programming activities for complex clinical studies, ensuring high-quality and timely outputs. You will collaborate with cross-functional teams, mentor junior programmers, and support regulatory interactions, while fostering quality assurance and innovation.

GSK

Hybrid Permanent

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working with internal and external teams to ensure studies are on time, on budget, and compliant with standards. Key responsibilities include monitoring study progress, drafting clinical documents, coordinating meetings, and managing study communications and supplies.

GSK Stevenage, United Kingdom

Hybrid Permanent

Programming Leader

The Programming Leader role involves overseeing project-level and study-level programming strategy and delivery for multiple complex studies in GSK's global pipeline. You will collaborate with cross-functional teams, ensure high-quality outputs, and champion the adoption of agile principles and new technologies to improve efficiency and data analysis.

GSK Stevenage, United Kingdom

Hybrid Permanent

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working closely with internal and external teams to ensure studies are delivered on time, on budget, and in compliance with standards. Key responsibilities include monitoring study progress, drafting clinical documents, coordinating meetings, and managing study communications and budgets.

GSK Poland

Hybrid Permanent

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working with study teams, vendors, and country colleagues to ensure studies are on time, on budget, and compliant with standards. Key responsibilities include monitoring study conduct, drafting clinical documents, coordinating meetings, and managing study communications and budgets.

GSK

Hybrid Permanent

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working with study teams, vendors, and country colleagues to ensure studies are on time, on budget, and compliant with standards. Responsibilities include monitoring study progress, drafting key documents, coordinating meetings, managing communications, and overseeing clinical supplies and budget tracking.

GSK

Hybrid Permanent