Latest Medical Services Jobs

Senior Medical Director, Oncology Clinical Development - GU

This role involves leading clinical development for genitourinary (GU) oncology programs within GSK’s pipeline, with responsibility for designing and executing phase 1–3 trials, ensuring scientific integrity, and supporting regulatory submissions. The Senior Medical Director will collaborate across functions and represent GSK externally with key experts and at medical meetings, driving data generation and strategic input for innovative oncology therapies.

GSK £284,250 – £473,750 pa

Hybrid Permanent

Senior Medical Director, Oncology Clinical Development - GU

This role involves leading clinical development for oncology, specifically genitourinary (GU) cancers, within GSK’s global portfolio. The Senior Medical Director will design and execute Phase 1–3 trials, provide medical oversight, interpret clinical data, and collaborate with internal teams and external experts to support regulatory submissions and product lifecycle management. The position requires deep expertise in GU oncology and strong leadership in a matrixed, science-driven environment.

GSK US$284,250 – US$473,750 pa

On-site Permanent

Executive Director, Oncology Search & Evaluation

This role involves leading oncology business development and licensing initiatives at GSK by identifying and evaluating external innovation opportunities. The Executive Director will lead due diligence, build strategic partnerships with biotech firms, and present investment recommendations to senior leadership. It requires deep scientific expertise, deal-making experience, and the ability to navigate complex cross-functional environments to advance GSK’s oncology pipeline.

GSK £229,350 – £382,250 pa

Hybrid Permanent

Senior Director RIIRU & TDS Strategy

This role leads high-impact strategic initiatives within GSK’s Respiratory Immunology and Inflammation Research Unit and Translational and Development Sciences organisation. The Senior Director will shape asset and portfolio strategy, interpret clinical and external data to inform investment decisions, and support governance processes at the R&D Leadership and Executive Committee levels. The position acts as a key interface with external partners and drives priority technology programmes while mentoring junior team members.

GSK United Kingdom

Hybrid Permanent

Senior Director / Director, Non-Clinical Safety Project Specialist

This role leads non-clinical safety strategy across drug discovery and development, integrating scientific data to inform project decisions, regulatory submissions, and risk assessment. The specialist provides expert guidance on safety profiling, candidate selection, and translational planning, while mentoring teams and shaping regulatory narratives. They work cross-functionally to ensure robust safety evaluation for small molecules and biologics through clinical and post-market stages.

GSK £224,400 – £374,000 pa

On-site Permanent

Senior Director / Director, Non-Clinical Safety Project Specialist

This role leads non-clinical safety strategy across drug discovery and development, integrating scientific data to inform project decisions, regulatory submissions, and risk assessment. The position involves mentoring teams, shaping translational plans, and providing expert input on safety profiling and candidate selection. It plays a key part in regulatory strategy and cross-functional leadership within a global biopharma environment.

GSK £224,400 – £374,000 pa

Hybrid Permanent

Director, Government Affairs and Advocacy - Europe and International

Director, Government Affairs and Advocacy – Europe and International ViiVAbout ViiVWe are a specialist pharmaceutical company 100% dedicated to developing medicines to treat and prevent HIV. As the pioneers in HIV innovation, we constantly look to push the boundaries of...

GSK United Kingdom

Molecule Steward

This role involves providing end-to-end technical leadership for a pharmaceutical product across its lifecycle, from development through commercial manufacturing. The Molecule Steward ensures product quality, manufacturability, and regulatory compliance by leading cross-functional teams, defining control strategies, and driving continuous improvement initiatives across the global supply chain.

GSK United States

Hybrid Permanent

Product Owner, Clinical Trial Site Management

This role involves leading AI-first product development for clinical trial site management systems at GSK, focusing on transforming how trials are conducted from feasibility through close-out. The Product Owner will drive strategy, adoption, and innovation across site-facing and internal operational platforms, using AI to enhance processes like contracting, budgeting, and monitoring. The role emphasizes responsible AI integration in a regulated GxP environment, with strong stakeholder collaboration across R&D operations and technology teams.

GSK United Kingdom

Hybrid Permanent

Team Lead, Therapeutic Area Quality

The Team Lead, Therapeutic Area Quality, leads a team of Quality Business Partners, ensuring quality is integrated into R&D programs and projects. Key responsibilities include driving quality improvements, supporting health authority inspections, and contributing to the quality strategy and risk management.

GSK United Kingdom

On-site Permanent

Team Lead, Therapeutic Area Quality

The Team Lead, Therapeutic Area Quality, leads a team of Quality Business Partners, ensuring quality is integrated into R&D programs and projects. Responsibilities include driving quality improvements, supporting health authority inspections, and contributing to the global audit plan. The role also involves talent development and maintaining expertise in international regulations.

GSK

On-site Permanent

Team Lead, Therapeutic Area Quality

This role involves leading a team of Quality Business Partners to ensure quality is integrated into R&D programs and projects. Responsibilities include evaluating quality strategies, driving continuous improvements, and supporting health authority inspections. The role also focuses on talent development and maintaining expertise in international regulations.

GSK

On-site Permanent

Team Lead, Therapeutic Area Quality

This role involves leading a team of Quality Business Partners to ensure quality is integrated into R&D programs and projects. Responsibilities include driving quality improvements, supporting health authority inspections, and contributing to the quality strategy and risk management. The role requires a deep understanding of regulatory requirements and the ability to lead a global quality team.

GSK

On-site Permanent

SERM Scientific Director

The SERM Scientific Director at GSK leads the safety evaluation and risk management of oncology assets in clinical development. This role involves driving pharmacovigilance activities, evaluating safety data, and collaborating with cross-functional teams to ensure robust benefit-risk profiles and patient safety. The position requires significant experience in pharmacovigilance and a strong understanding of global regulations.

GSK

On-site Permanent

HR Business Partner - R&D Development Operations

At GSK, we unite science, technology and talent to get ahead of disease together. We are looking for an experienced and strategicHR Business Partner to join our Global Human Resources team, supporting ourDevelopment Operations organisation.This is an exciting opportunity to...

GSK United Kingdom