Observational Research Manager
Core
Design and execute pharmacoepidemiology studies to generate real-world evidence for product safety, benefit-risk assessment, and regulatory decision-making across East Asia.
Role type
Senior IC observational research manager (pharmacoepidemiology)
Builds
Real-world evidence studies, regulatory submissions, and scientific publications
Domain
Biopharmaceuticals / Pharmacoepidemiology
Required skills
Pharmacoepidemiology study design, causal inference methods, real-world data analysis, regulatory evidence generation, scientific writing, cross-functional collaboration
Preferred skills
Target trial emulation, causal roadmaps, secondary healthcare data analysis (claims, EMR, registries), East Asian language proficiency
Technologies
Real-world data sources (claims, electronic medical records, registries)
Responsibilities
Design and execute pharmacoepidemiology studies; Apply epidemiologic and causal inference methods; Lead interpretation of real-world evidence on adverse events and outcomes; Collaborate with global epidemiology, safety, and regulatory teams; Contribute to regulatory submissions and risk management activities; Develop study protocols, analysis plans, and peer-reviewed publications
Seniority
Senior, hands-on IC