Manager, US Real-World Evidence and Health Outcomes, Specialty Medicines, Hepatology & Immunology

GSK•Philadelphia, PA

2d•Hybrid

About The Position

This role will lead the design and delivery of real-world evidence and health outcomes work that supports product access and patient impact in the United States. The position involves working with cross-functional teams across medical, commercial, research and development, and external partners to generate timely, high-quality evidence. The company values people who are curious, collaborative, and clear communicators. This role offers strong growth, visible impact on strategy, and the chance to contribute to GSK’s mission of uniting science, technology and talent to get ahead of disease together.

Requirements

Master’s degree or higher in health economics, epidemiology, biostatistics, public health, or health services research.
2 or more years of experience designing, delivering, or managing real-world evidence or health outcomes studies.
Practical experience with US healthcare systems, payer evidence requirements, or health technology assessment.
Experience working in a matrix environment with cross-functional teams.
Experience managing external vendors or research partners and tracking project budgets and timelines.
Strong written and verbal communication skills with ability to present technical evidence to diverse audiences.

Nice To Haves

PhD or advanced scientific degree in a relevant field.
Experience with biostatistical/epidemiologic methods applied to RWE.
Experience contributing to or leading publications, abstracts, or payer dossiers.
Prior experience in the pharmaceutical or biotech industry, ideally in health economics or outcomes research.
Experience with large US real-world data sources (claims, electronic health records, registries).
Demonstrated ability to influence stakeholders and to translate evidence into clear payer and clinical messages.
Knowledge of specialty medicines, particularly in hepatology or immunology.

Responsibilities

Lead the development and execution of real-world evidence (RWE) and health outcomes studies to inform access, reimbursement, and clinical practice.
Translate stakeholder evidence needs into study concepts, protocols, analysis plans, and dissemination activities.
Manage study delivery, including timelines, vendor partners, budgets, quality control, and regulatory or compliance requirements.
Engage internal partners (medical affairs, market access, marketing, R&D) to align evidence plans with product strategy.
Present results clearly to internal and external audiences, including payers, health systems, and scientific meetings; support publications and technical reports.
Maintain knowledge of US payer, health technology assessment and real-world data sources to recommend fit-for-purpose approaches.