Latest Medical Affairs Partner - Nephrology & R Jobs

Project Specialist (External Manufacturing-Drug Product)

The role involves managing technology transfer projects for external manufacturing of drug products, coordinating between GSK and Contract Manufacturing Organisations (CMOs). The specialist ensures timely delivery of critical path activities, aligns internal and external stakeholders, and maintains governance across procurement, quality, technical, and supply functions, particularly for sterile drug products like monoclonal antibodies and vaccines.

GSK €69,600 – €116,000 pa

Hybrid Permanent

ViiV Healthcare (GSK) Director, Clinical Pharmacology

This role involves leading clinical pharmacology strategy across HIV drug development programs, applying PK/PD and pharmacometric modeling to inform study design, regulatory decisions, and development pathways. The Director will mentor project leads, collaborate with cross-functional teams, and serve as a scientific expert in modeling and simulation to advance ViiV’s mission-driven HIV research from early to late-stage development.

GSK United States

Hybrid Permanent

ViiV Healthcare (GSK) Director, Clinical Pharmacology

This role involves providing scientific leadership in clinical pharmacology to shape drug development programs for HIV treatments. The Director will apply PK/PD, pharmacometrics, and model-informed drug development approaches to guide study design, regulatory strategy, and key decisions across early to late-stage development. Collaboration with cross-functional teams including clinical, regulatory, biostatistics, and CMC is central to advancing innovative therapies in a mission-driven environment focused on eradicating HIV.

GSK

Hybrid Permanent

ViiV Healthcare (GSK) Director, Clinical Pharmacology

This role involves leading clinical pharmacology strategy across HIV drug development programs, applying PK/PD, pharmacometrics, and modeling to inform study design, regulatory decisions, and development pathways. The Director will mentor project leads, collaborate with cross-functional teams, and serve as a scientific expert in model-informed drug development, contributing to breakthroughs in HIV treatment and prevention.

GSK

Hybrid Permanent

Executive Director, Oncology Search & Evaluation

This role leads oncology business development and licensing initiatives at GSK, focusing on identifying and evaluating external innovation opportunities. The Executive Director will conduct scientific and strategic due diligence, build partnerships with biotech firms, and present investment cases to senior leadership, playing a central role in shaping GSK’s oncology pipeline.

GSK United States US$229,350 – US$382,250 pa

Hybrid 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

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