Latest Clinical Research Associate Jobs

Manager, Translational Biomarker Data Pathways & Re-use

This role involves leading the setup, stabilization, and scaling of end-to-end translational data pathways at GSK. Key responsibilities include ensuring biomarker datasets are reusable, accessible, and aligned with translational decision-making, while also identifying and resolving systemic barriers and developing repeatable processes.

GSK

Hybrid Permanent

Senior Scientist ETCT

The Senior Scientist will work within the ETCT Biology Unit, contributing to pre-clinical and early clinical biologics programs. Responsibilities include designing and executing experiments, providing input on pharmacokinetics and non-clinical safety, and mentoring junior scientists.

GSK Stevenage, United Kingdom

Hybrid Permanent

Director, Medical Insights

The Director, Medical Insights role involves shaping and implementing Medical Insights processes, collaborating with various stakeholders to generate actionable insights, and embedding these insights into medical decision-making. The role focuses on leveraging advanced analytics and AI to translate complex medical data into strategic decisions, ensuring consistency and value across Pfizer’s medical portfolio.

Pfizer

On-site Permanent

Director, Medical Insights

The Director, Medical Insights role involves shaping and implementing processes to generate high-quality medical insights. Key responsibilities include developing strategies, prioritizing use cases, and applying advanced analytics and AI to inform medical decision-making. The role also focuses on embedding insights into core medical processes and collaborating with various stakeholders to ensure effective use of insights.

Pfizer

On-site Permanent

Global Labelling Associate Director, Content (Cardiovascular, Renal & Metabolism)

This role involves developing and maintaining global labelling strategies and documents for cardiovascular, renal, and metabolic products. You will lead cross-functional discussions, present labelling proposals, and ensure compliance with regulatory requirements across global markets.

Novartis London, United Kingdom

Hybrid Permanent

Trial Vendor Senior Manager

This role involves managing all vendor-related aspects of global clinical trials, ensuring study outcomes are delivered within schedule, budget, and quality standards. The Senior Manager will collaborate with the Vendor Start-up Manager and other team members, oversee vendor interfaces, and manage risks and performance.

Novartis London, United Kingdom

Hybrid Permanent

Senior Director, Head, Vaccines and Infectious Diseases, Global Epidemiology and RWE

This role involves providing strategic leadership in epidemiology, leading a global team of VID epidemiologists, and collaborating across R&D functions. Responsibilities include designing and executing epidemiological studies, contributing to regulatory submissions, and driving innovation in methodologies and tools.

GSK

Hybrid Permanent

Director, Global Real-World Evidence & Health Outcomes Scientist, Oncology

This role involves planning, designing, and executing real-world evidence studies to support the commercial success and market positioning of GSK's oncology products. The Director will collaborate with internal and external stakeholders to ensure the generation of high-quality, scientifically credible evidence that meets regulatory and payer requirements.

GSK

On-site Permanent

Director, Global Real-World Evidence & Health Outcomes Scientist, Oncology

This role involves planning and executing real-world evidence studies to support the commercial success of GSK's oncology products. The Director will work closely with medical and commercial teams to ensure that evidence is aligned with regulatory and payer requirements, and will be responsible for managing timelines, budgets, and deliverables.

GSK

On-site Permanent

Director, Global Real-World Evidence & Health Outcomes Scientist, Oncology

This role involves planning and executing real-world evidence studies to support the launch and market positioning of GSK's oncology products. The Director will work closely with medical and commercial teams to ensure the generation of high-quality evidence that meets regulatory and payer requirements, driving successful patient access and commercial outcomes.

GSK

On-site Permanent

Director, Global Real-World Evidence & Health Outcomes Scientist, Oncology

This role involves planning and executing real-world evidence studies to support the launch and commercial success of GSK's oncology products. The Director will collaborate with internal and external stakeholders to ensure the generation of high-quality, scientifically credible evidence that meets regulatory and market requirements.

GSK

On-site Permanent

Medical Lead - Respiratory

This role involves leading the medical strategy for GSK's specialty respiratory portfolio, ensuring patient needs are at the forefront. Responsibilities include managing a medical therapy team, developing strategic plans, and engaging with healthcare professionals and regulatory bodies.

GSK United Kingdom

Hybrid Permanent

ViiV Healthcare (GSK) Statistics Leader

The Statistics Leader at ViiV Healthcare will provide statistical leadership and support for one or more HIV treatment programs. Responsibilities include managing statistical contributions, influencing project strategies, and ensuring the scientific integrity of data dissemination. The role involves cross-functional collaboration, advanced analytics, and mentoring team members.

GSK

On-site Permanent

ViiV Healthcare (GSK) Clinical Development Manager

The Clinical Development Manager at ViiV Healthcare provides scientific leadership and direction for clinical development programs, focusing on the design and execution of high-quality studies. This role involves collaborating with cross-functional teams to ensure study protocols meet strategic objectives, overseeing data collection and analysis, and contributing to regulatory reporting and scientific outputs.

GSK United States

On-site Permanent

ViiV Healthcare (GSK) Clinical Development Manager

The Clinical Development Manager at ViiV Healthcare is responsible for providing scientific leadership and direction in the design and development of high-quality clinical studies. This role involves collaborating with cross-functional teams to ensure the accuracy and timeliness of study results, contributing to regulatory reporting, and creating scientific outputs for publications and presentations.

GSK

On-site Permanent