Director, Respiratory Biologics - Global Real-World Evidence & Health Outcomes Research
GSK
August 14, 2026
Remote friendly (Philadelphia, PA)
United States
Clinical Research and Development
Role: Director, Global Real-World Evidence & Health Outcomes Research (Respiratory Biologics portfolio)
Responsibilities:
- Plan, design, and execute real-world evidence (RWE) and qualitative research studies; manage timelines, deliverables, and budget; ensure quality and sign off on specifications, protocols, analysis plans, and final outputs (reports, abstracts, posters, manuscripts) per SOPs.
- Align local data generation with the global data generation plan and enable global-local information sharing.
- Partner with cross-functional stakeholders across countries (medical, market access, R&D, commercial) to ensure strategic alignment and collaboration.
- Engage data generation partners across global and country levels; support study design, execution, translation, and dissemination across indications.
Work arrangement:
- Hybrid; located in the United States; travel as needed.
Required qualifications/skills:
- Master’s in health outcomes/PROMs, health economics, epidemiology, pharmacy, health, or life sciences.
- 10+ years in pharmaceutical industry (preferably multinational).
- Evidence generation planning and workshop development; detailed project/program planning.
- Experience delivering studies and communications in fast-paced environments.
- RWE experience (prospective, cross-sectional, retrospective cohort) and patient-reported outcomes research.
- Knowledge of global/local healthcare markets, HTA agencies, and reimbursement decision-making.
- Applied experience using evidence for HTA submissions and/or reimbursement/medical engagement.
- Ability to communicate technical results to diverse audiences (incl. senior leaders).
Preferred:
- PhD/PharmD (or equivalent); asthma HEOR experience.
- Consulting perspective; leading client communications.
Compensation/benefits (US): Base salary $185,250–$308,750; annual bonus; share-based long-term incentive; health/insurance, retirement, paid holidays/vacation, caregiver/parental and medical leave.
Application instructions:
- Apply if interested and qualified.
Responsibilities:
- Plan, design, and execute real-world evidence (RWE) and qualitative research studies; manage timelines, deliverables, and budget; ensure quality and sign off on specifications, protocols, analysis plans, and final outputs (reports, abstracts, posters, manuscripts) per SOPs.
- Align local data generation with the global data generation plan and enable global-local information sharing.
- Partner with cross-functional stakeholders across countries (medical, market access, R&D, commercial) to ensure strategic alignment and collaboration.
- Engage data generation partners across global and country levels; support study design, execution, translation, and dissemination across indications.
Work arrangement:
- Hybrid; located in the United States; travel as needed.
Required qualifications/skills:
- Master’s in health outcomes/PROMs, health economics, epidemiology, pharmacy, health, or life sciences.
- 10+ years in pharmaceutical industry (preferably multinational).
- Evidence generation planning and workshop development; detailed project/program planning.
- Experience delivering studies and communications in fast-paced environments.
- RWE experience (prospective, cross-sectional, retrospective cohort) and patient-reported outcomes research.
- Knowledge of global/local healthcare markets, HTA agencies, and reimbursement decision-making.
- Applied experience using evidence for HTA submissions and/or reimbursement/medical engagement.
- Ability to communicate technical results to diverse audiences (incl. senior leaders).
Preferred:
- PhD/PharmD (or equivalent); asthma HEOR experience.
- Consulting perspective; leading client communications.
Compensation/benefits (US): Base salary $185,250–$308,750; annual bonus; share-based long-term incentive; health/insurance, retirement, paid holidays/vacation, caregiver/parental and medical leave.
Application instructions:
- Apply if interested and qualified.