Associate Director - Global Epidemiology & RWE

GSK; Upper Providence (Delaware County); Hybrid; USD 149,000 - 249,000; Full time

Benefits offered by this job

Annual bonus

Healthcare and wellbeing programs

Pension plan membership

Shares and savings programme

Paid caregiver/parental and medical/lo

Paid holidays

Vacation

Job summary

GSK is seeking an Associate Director of Global Epidemiology and Real-World Evidence to lead epidemiology efforts across development and lifecycle activities. You will work with clinical development, safety, regulatory, outcomes, and commercial teams to design and deliver studies using real-world data, registries, and linked sources.

You will guide study design, data needs, and analysis plans while communicating findings to asset teams.

Qualifications

• Master's degree in Epidemiology, Public Health, Biostatistics, or related quantitative discipline.

Responsibilities

• Lead epidemiology programs for one or more assets or disease areas, creating strategy and timelines with cross-functional partners.
• Design, oversee, and deliver observational and database studies using real-world data, registries, and linked sources.
• Provide timely scientific advice on study design, data needs, analysis plans, and interpretation of results to asset teams.
• Manage external partners, vendors, budgets, and timelines to ensure high-quality, on-time study delivery.
• Prepare regulatory documents, technical reports, and publications that clearly communicate study findings.
• Build capability by sharing methods, best practice, and learnings across teams.

Skills

Applied epidemiology

Observational studies

Healthcare database analyses

Cross-functional collaboration

Communication skills

Education

Master's degree in Epidemiology / Public Health / Biostatistics

Doctoral degree acceptable

PhD in Epidemiology / Public Health / Biostatistics

Job description

GSK is seeking an Associate Director of Global Epidemiology and Real-World Evidence to lead epidemiology efforts across development and lifecycle activities. You will work with clinical development, safety, regulatory, outcomes, and commercial teams to design and deliver studies using real-world data, registries, and linked sources.

You will guide study design, data needs, and analysis plans while communicating findings to asset teams.