Director, Real-World Evidence & Health Outcomes, mRNA Vaccines in London

The CPO organization partners closely with R&D and Commercial to translate cutting-edge science into measurable health outcomes, grounded in the patient voice and external insights from healthcare systems and decision-makers worldwide. Joining CPO means working across the full product lifecycle and collaborating with diverse expert teams – from Patients & External Environment and Medical Planning to Data Generation, Scientific Communications, Medical Impact, Proactive Risk Ownership and Integrated Evidence Strategy – to ensure robust evidence, clear medical insight and responsible risk ownership shape strategy and execution at scale. It’s a highly visible, purpose-driven environment where your expertise can directly influence how innovative therapies are developed, communicated and used to improve lives around the world.

The Director, Real-World Evidence & Health Outcomes (RWE-HO), mRNA Vaccines will provide scientific and strategic leadership for the development and delivery of real-world evidence supporting GSK’s mRNA vaccine portfolio, with a primary focus on influenza. The role will shape evidence generation across late-stage development, launch and post-marketing phases, with particular responsibility for post-marketing vaccine effectiveness studies in the United States.

Working in a global, cross-functional environment, the Director will translate recommendation and access evidence needs into scientifically rigorous and operationally feasible research. The role requires deep expertise in US vaccine effectiveness research, influenza epidemiology, real-world data and causal methods, together with the ability to influence asset strategy and lead complex external collaborations.

Responsibilities

• Lead and contribute to the integrated RWE-HO strategy for mRNA influenza vaccines, aligned with clinical development, medical, regulatory and commercialization priorities.
• Translate strategic evidence gaps into clear research questions and fit-for-purpose study designs across pre-launch, launch and post-marketing phases.
• Provide expert scientific input to governance decisions, investment choices, evidence prioritization and risk mitigation.
• Lead the design, implementation and interpretation of post-marketing influenza vaccine effectiveness studies in the United States and other geographies.
• Ensure studies meet appropriate standards of scientific rigor, transparency, reproducibility and fitness for their intended decision-making purpose.
• Build productive collaborations with US academic investigators, healthcare systems, data partners and vaccine effectiveness research networks.
• Partner effectively with Clinical Development, Epidemiology, Medical Affairs, Regulatory, Safety, Biostatistics, Market Access, Data Science and Commercial teams.
• Lead multiple complex projects, budgets and external research collaborations, ensuring quality, timely delivery and appropriate escalation of risks.
• Influence senior stakeholders without direct authority and communicate complex epidemiological concepts in a clear, decision-focused manner.
• Mentor colleagues and contribute to strengthening RWE-HO capabilities, standards and innovation across the organization.

Basic Qualifications:

• PhD, ScD, DrPH, MD, PharmD, MPH or equivalent advanced degree in epidemiology, public health, pharmacoepidemiology, health outcomes research or a related quantitative discipline.
• 5+ years experience in real-world evidence, epidemiology or health outcomes research within the pharmaceutical or vaccine industry, academia, public health or a comparable environment.
• Experience designing, conducting and interpreting post-marketing vaccine studies in the United States.
• Research experience with vaccine effectiveness studies.
• Experience using large US healthcare databases, including administrative claims, electronic health records or linked real-world datasets.
• Experience leading complex studies from concept through delivery, interpretation and scientific dissemination.
• Demonstrated effectiveness in global, cross-functional matrix teams and in managing internal and external stakeholders.

Preferred Qualifications:

• Direct experience with influenza vaccine effectiveness studies in the United States.
• Experience with US Medicare, commercial claims, EHR and linked claims/EHR data.
• Knowledge of US influenza vaccination recommendations, vaccine delivery and healthcare systems.
• Experience studying severe influenza, hospitalization, cardiovascular complications or other downstream outcomes.
• Experience leading global evidence-generation plans or multi-country observational studies.

What success looks like

The successful candidate will combine deep technical expertise with strategic asset-level thinking. They will design credible US post-marketing studies, anticipate the methodological challenges specific to influenza, and convert complex evidence needs into practical solutions. They will be a trusted scientific partner who can influence decisions, build external credibility and deliver evidence that supports the value and appropriate use of GSK’s mRNA vaccines.

Are you ready to help shape the future of vaccination with meaningful evidence that impacts patient care? If this role speaks to your passion and experience, we encourage you to apply and grow with us at GSK. Your contribution matters.

Skills

• Cross-Functional Leadership
• Digital Fluency
• Enterprise Thinking
• Evidence Based Decision Making
• Flexible Mindset
• High Impact Communication
• Launch Excellence
• Patient Journey

If you require an accommodation or other assistance to apply for a job at GSK, please contact the appropriate Recruitment Staff by emailing us at.

GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.