VP, Cluster Head RSV Vaccine

At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-edge technology to transform people’s lives. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients’ needs and have the highest probability of success.

We’re uniting science, technology, and talent to get ahead of disease together.

The Vaccines/Infectious Diseases (Vx/) Cluster Head is a core member of the Vx/ Clinical Science Leadership Team and acts as the single point of accountability for the integrated Clinical Development Plan (CDP), contributing to the disease area strategy with input from both internal GSK leaders and external experts, including academic thought leaders and regulatory authorities. This role is responsible for ensuring the delivery of robust CDPs that explore new areas of interest and alternative development pathways, enabling smart risk‑taking for assets within the disease area.

The Vx/ Science Cluster Head drives innovation in the design of CDPs and study protocols, accessing world‑class expertise through collaboration and harnessing digital, technological, and statistical tools to support all development stages. They provide Clinical/Medical Governance, managing and mentoring clinical staff, ensuring proper training and compliance, and fostering Clinical Development Excellence through talent identification, recruitment, and retention. Additionally, this role ensures the quality of all clinical deliverables, including documents, submissions, and clinical data, through peer review and knowledge sharing, and oversees high‑quality presentations to regulatory bodies.

The Vx/ Sciences Cluster Head also acts as a Data Steward for the disease area, manages resources across clinical projects, and leads project oversight to ensure timely delivery of clinical programs.

• Accountable for the clinical development planning of assets within their disease area, ensuring alignment with key clinical stakeholders and providing clinical/medical overview over the CDP.
• Lead interpretation and critical evaluation of study results with respective clinical development leaders.

• Accountable for allocating appropriate disease expert input to the appropriate Project Team (e.g. Vaccine Development Team) to support the delivery of Vaccines target profiles.
• Manage and allocate clinical personnel across projects and programs within the disease area portfolio, ensuring appropriate resourcing.

• Accountable to work with the Head of Clinical Sciences to set forward the disease area strategy for clinical development, ensuring it is informed by world‑class expertise and aligned with business goals.
• Lead the external scientific insight strategy for the disease area, incorporating input from scientific experts, patients, physicians, payers, and regulators.

• Accountable for the accuracy and scientific integrity of clinical input to regulatory documents and meetings with global impact, overseeing asset‑level Clinical Development Leaders.
• Ensure the delivery of high‑quality regulatory documentation and packages to support desired indications.

• Accountable for providing globally integrated medical governance of clinical research, ensuring scientific integrity and overall safety of study subjects.
• Support interactions with Medical Affairs and Global Clinical Safety and Pharmacovigilance leaders to maintain robust medical governance.

• Enhance delivery and improve end‑to‑end pipeline productivity by driving clear disease area strategies, aligned Vaccine product profiles, and Clinical Development Plans.
• Drive simplification and reduce complexity across R&D, exploring opportunities for optimal resourcing models and risk…