Director, Global RWE-HO, Oncology

GSK

Director for Global Real-World Evidence & Health Outcomes at GSK. Managing studies to support drug market success and patient access across various stakeholders.

Posted 7/6/2026full-timeUpper Providence • Pennsylvania • 🇺🇸 United StatesLeadWebsite

About the role

Key responsibilities & impact

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 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 experts (medical affairs, clinical, commercial/market access) and external experts as needed in support of the asset team.
Translate needs for evidence into study concepts in alignment with strategic objectives and vision for the asset, e.g. development of study protocols and proposing innovative and cost-effective ways of developing and executing studies.
Develop and maintain a good working knowledge of real-world data resources, existing partnerships and public initiatives and become the point person for select sources to advise on their suitability to address given research questions.
Develop a deep understanding of customers’ needs, including clinicians and HTA requirements, and their acceptance of different types of evidence and impact of that evidence to their decision making.
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 cross-functional collaboration and communication.
Ensure key stakeholders, including TA aligned business leaders, are regularly 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.

Requirements

What you’ll need

MSc, or equivalent in health outcomes, health economics, epidemiology, pharmacy, health or life sciences.
3+ years of experience working in the pharmaceutical industry, preferably in a multi-national company.
Experience in planning and delivering individual projects, managing budgets and working within a matrix setting.
A 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 HTA submissions, reimbursement and/or medical engagements.
A track record of delivering robust payer evidence and credibility to engage 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, in region and local markets.
Experience in communicating technical and complex concepts and results to various audiences to impact decision-making.

Benefits

Comp & perks

Health insurance
401(k) matching
Flexible working hours
Paid time off
Remote work options

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

EpidemiologyHealth EconomicsData AnalysisStudy Protocol DevelopmentBudget ManagementProspective Observational StudiesRetrospective Cohort StudiesDatabase AnalysisChart ReviewsEvidence Utilization

Soft Skills

CommunicationCollaborationRelationship BuildingStrategic ThinkingProblem Solving

Certifications

MSc in Health OutcomesMSc in Health EconomicsMSc in EpidemiologyMSc in PharmacyMSc in Health or Life Sciences