Director, Global Real-World Evidence & Health Outcomes Research – Hematology-Oncology

GSK

Director of Global Real-World Evidence & Health Outcomes Research for hematology-oncology at GSK. Leading studies to ensure evidence supports new medicines for market success.

Posted 7/7/2026full-timeUpper Providence • Pennsylvania • 🇺🇸 United StatesLead💰 $185,250 - $308,750 per yearWebsite

About the role

Key responsibilities & impact

Ensure each medicine GSK brings to market is supported by scientifically credible, high quality evidence.
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.
Identify resources, references and analyses to inform scientific design and advise internal 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.
Develop and maintain a good working knowledge of real-world data resources, existing partnerships and public initiatives.
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 internal stakeholder groups across medical, market access, R&D and commercial.
Ensure key stakeholders 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.

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.
Experience in oncology or hematology.

Benefits

Comp & perks

Health care and other insurance benefits (for employee and family)
Retirement benefits
Paid holidays
Vacation
Paid caregiver/parental and medical leave
Annual bonus
Eligibility to participate in share-based long-term incentive program

ATS Keywords

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Hard Skills & Tools

Study DesignData AnalysisBudget ManagementEvidence UtilizationProject PlanningEpidemiologyHealth EconomicsPharmacyClinical ResearchDatabase Analysis

Soft Skills

CollaborationCommunicationRelationship BuildingStakeholder EngagementBest Practice Sharing

Certifications

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