Director, Global Real-World Evidence & Health Outcomes Scientist, Oncology

For drugs to be successful, robust health outcomes data must support launch optimization, reimbursement, and market positioning throughout the product lifecycle. The role of Director, Global Real-World Evidence & Health Outcomes Research Scientist is critical to support evidence generation that drives competitiveness, value propositions, and value‑based pricing for GSK medicines.

Responsibilities

• Plan, design, and execute multiple studies for a given asset and manage timelines, deliverables, and budget.
• Assure quality of deliverables, including review and sign‑off of project specifications, protocols, data analysis plans, final study reports, abstracts, posters, and manuscripts in adherence to SOPs.
• Identify resources, references, and analyses to inform scientific design and advise internal and external experts as needed.
• Translate evidence needs into study concepts aligned with strategic objectives and the asset vision.
• Develop and maintain knowledge of real‑world data resources, existing partnerships, and public initiatives to advise on suitability for research questions.
• Develop a deep understanding of customers’ needs, including clinicians and HTA requirements, and their acceptance of different types of evidence.
• Collaborate with internal teams and participate in best‑practice sharing sessions across the non‑interventional study organization.
• Build strong working relationships with stakeholder groups across medical, market access, R&D, and commercial to ensure strategic alignment and optimal collaboration.
• Ensure key stakeholders are updated on plans through periodic reporting.
• Develop excellent working relationships with external thought leaders to ensure appropriate methods and research agendas are applied, in accordance with GSK policies.

Basic Qualification

• MSc, or equivalent, in health outcomes, health economics, epidemiology, pharmacy, health or life sciences.
• 5+ years of experience in the pharmaceutical industry, preferably in a multi‑national company.
• Experience in planning and delivering projects, managing budgets, and working within a matrix setting.
• History of designing a variety of RWE studies including prospective observational studies, cross‑sectional and retrospective cohort studies, chart reviews, and database analyses.
• Proficiency in utilizing evidence for the development of global HTA submissions, reimbursement, and/or medical engagements.
• Track record of delivering robust payer evidence and engaging meaningfully with external experts and leaders in the field.
• Expertise with the diversity and complexity of healthcare markets, health technology assessment agencies, and reimbursement decision making globally, regionally, and locally.
• Experience communicating technical and complex concepts and results to various audiences to impact decision‑making.
• Experience in oncology.

Preferred Qualification

• Advanced scientific degree, e.g., PhD, PharmD, or equivalent in Health Economics, Outcomes Research, Epidemiology, or related field.
• Experience in global and country roles in oncology.

Compensation and Benefits

• Salary range for US locations: $204,000–$340,000 annually, adjusted for location and experience.
• Annual bonus and eligibility for share‑based long‑term incentive program.
• Benefits include health care and insurance for employee and family, retirement benefits, paid holidays, vacation, and paid caregiver/parental and medical leave.

Equal Opportunity Statement

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.