Latest GSK Jobs

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

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

Regional Medical Advisor

The EU and International Regional Medical Advisor role involves representing the business voice, leading the implementation of Medical Affairs processes, and supporting data generation across the EU and International regions. You will collaborate with local operating companies, conduct impact assessments, and serve as a subject matter expert in innovative processes.

GSK

On-site Permanent

VIDRU Business Programs Strategy Director

The VIDRU Business Programs Strategy Director role involves translating the vision and priorities of the Vaccines and Infectious Diseases Research Unit into coherent, enterprise-wide programs. Key responsibilities include strategic planning, cross-functional collaboration, and ensuring the delivery of measurable business value through data-driven insights and effective governance.

GSK United States

Hybrid Permanent

VIDRU Business Programs Strategy Director

The VIDRU Business Programs Strategy Director role involves translating the vision and priorities of the Vaccines and Infectious Diseases Research Unit into coherent, enterprise-wide programs. Key responsibilities include strategic planning, cross-functional collaboration, data-driven decision-making, and leading matrix teams to deliver measurable business value and support GSK's goals for innovation, trust, and performance.

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

Head of RII or Oncology Programming

This role involves leading the clinical data programming for GSK's Respiratory, Immunology & Inflammation or Oncology Research Unit. Responsibilities include setting high standards for data quality, driving innovation with technologies like Generative AI, and collaborating with cross-functional teams to accelerate the development and submission of new medicines and vaccines.

GSK United Kingdom

On-site Permanent

Head of RII or Oncology Programming

This role involves leading the clinical data programming for GSK's Respiratory, Immunology & Inflammation or Oncology Research Unit. Responsibilities include setting high standards for data quality, driving innovation with technologies like Generative AI, and collaborating with cross-functional teams to accelerate the development and submission of medicines and vaccines.

GSK

On-site Permanent

Head of RII or Oncology Programming

This senior leadership role involves overseeing the transformation of clinical data into regulatory-ready evidence for GSK's Respiratory, Immunology & Inflammation, or Oncology Research Units. The Head of Programming will lead a global team, drive strategic initiatives, and champion innovation in clinical programming, ensuring high standards of quality and compliance.

GSK

On-site Permanent

Clinical Trial Supply Manager

This role involves managing the end-to-end clinical supply chain for GSK’s global R&D studies, translating protocols into operational supply strategies, and ensuring timely delivery of investigational products. The manager will coordinate across depots, logistics partners, and clinical teams to maintain supply continuity, minimise waste, and support study milestones across phases I–IV. It requires strong planning, risk management, and GxP compliance in a patient-focused, global trial environment.

GSK Belgium €69,600 – €116,000 pa

On-site Permanent

Clinical Trial Supply Manager

This role involves managing the clinical trial supply chain for GSK's global R&D studies, translating protocols into operational supply strategies, and ensuring timely delivery of investigational products. The manager coordinates across depots, logistics partners, and internal teams to maintain compliance, minimise waste, and support study milestones across all phases of clinical development.

GSK €48,375 – €116,000 pa

On-site Permanent

Clinical Trial Supply Manager

This role involves managing the end-to-end clinical supply chain for GSK's global R&D trials, translating protocols into supply strategies, and ensuring timely delivery of investigational products. The manager will lead supply planning, coordinate with depots and logistics partners, and act as the primary link between clinical teams and supply operations across Phase I–IV studies. Emphasis is placed on risk-adjusted, patient-focused planning and continuous improvement in compliance with GxP and regulatory standards.

GSK £48,375 – £116,000 pa

On-site Permanent