Global Epidemiology & Real-World Evidence Leader

Gsk; Cambridge (MA); Hybrid; GBP 112,000 - 187,000; Full time

Benefits offered by this job

Healthcare

Pension plan

Annual bonus

Shares and savings programme

Hybrid work model

Job summary

GSK is seeking an Associate Director of Global Epidemiology and Real-World Evidence in a hybrid US-based role. You will lead epidemiology studies across assets, collaborating with clinical development, safety, regulatory, and outcomes teams to inform decision-making.

You will design studies using real-world data, manage external partners, and produce regulatory documents and publications. Strong communication and methodological excellence are essential.

Qualifications

• Master's degree in Epidemiology, Public Health, Biostatistics, or related quantitative discipline. Doctoral degree acceptable.
• Minimum 5 years of applied epidemiology or outcomes research experience.
• Proven experience designing and delivering observational studies or healthcare database analyses.
• Experience working in a matrix environment with cross-functional teams.

Responsibilities

• Lead epidemiology programs for assets or disease areas with strategy and timelines.
• Design and deliver observational and database studies using real-world data and linked sources.
• Provide scientific advice on study design, data needs, analysis plans, and interpretation of results.
• Manage external partners, vendors, budgets, and timelines for study delivery.
• Prepare regulatory documents and publications communicating study findings clearly.
• Share methods and best practices across teams to build capability.

Skills

Epidemiology

Data analysis

Communication

Cross-functional collaboration

Education

Master's degree in Epidemiology/Public Health/Biostatistics

PhD in Epidemiology (preferred)

Tools

R

SAS

Data linkage

Job description

GSK is seeking an Associate Director of Global Epidemiology and Real-World Evidence in a hybrid US-based role. You will lead epidemiology studies across assets, collaborating with clinical development, safety, regulatory, and outcomes teams to inform decision-making.

You will design studies using real-world data, manage external partners, and produce regulatory documents and publications. Strong communication and methodological excellence are essential.