Associate Director, Epidemiology (HPV)
$95,460–$132,460 year
Hybrid · Montréal, Quebec, Canada or Upper Providence, Pennsylvania, United States
Job Summary
Associate Director, Epidemiology (HPV) at GSK will provide scientific leadership in disease epidemiology leveraging real-world data to generate credible real-world evidence (RWE) across vaccine development. Responsibilities include leading an epidemiology program for at least one asset/disease area, developing a Global Epidemiology Plan, guiding cross-functional teams, delivering complex observational studies, identifying vendors and data sources for innovative solutions, disseminating epidemiology findings through regulatory documents and publications, and representing GSK in interactions with regulators and international conferences. The role requires a Master’s degree in a quantitative field, experience in pharmacoepidemiology or outcomes research, matrix-team collaboration, and strong communication with regulators. Preferred qualifications include a PhD and 1+ year in pharma or equivalent, experience with multiple real-world data sources, advanced quantitative methods, and peer-reviewed publications. The position is hybrid with on-site and remote work three days per week; salary CAD 129,000 to CAD 179,000 (published as location-specific ranges). The posting notes pay transparency and benefits information and emphasizes a globally inclusive culture.
Required Qualifications
- Master’s degree in Epidemiology, Public Health, Biostatistics, or a related quantitative discipline
- Epidemiological experience and ability to influence internal and external stakeholders
- Experience applying epidemiologic methods in pharmacoepidemiology, clinical development, or outcomes research
- Experience designing and delivering observational and database studies, including protocol development and analysis oversight
- Experience working in a matrix environment and influencing multidisciplinary teams
- Experience providing the delivery of increasingly complex epidemiological studies, including regulatory requirements
- Experience applying epidemiology methods and study design knowledge in execution of post-approval studies
- Experience working with external regulatory requirements and scientific landscape around RWE
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