This role provides epidemiology leadership for real-world studies including natural history of disease and post-market surveillance for global pharmaceutical clients
Job Summary
This role provides epidemiology leadership for real-world studies including natural history of disease and post-market surveillance for global pharmaceutical clients.
The position involves independently designing complex methodologically sound studies and authoring sections for regulatory submissions such as orphan designation applications.
Candidates will benefit from home-based remote working opportunities, flexible schedules, and a focus on bringing new therapies to market rather than project budgets.
Matching Summary
This role provides epidemiology leadership for real-world studies including natural history of disease and post-market surveillance for global pharmaceutical clients.
Salary
Base: $105,800.00 - $350,300.00 annualized; Bonus/Equity: Dependent on position offered; Benefits: Range of health and welfare benefits included
Skills & Requirements
Must-have
PhD in epidemiology or related field
7 years relevant pharmacoepidemiology experience
Design complex observational studies
Author regulatory submission documents
Proficiency in SAS, R, or similar languages
Nice-to-have
Experience with RNAi therapeutics
Strong medical writing skills
Leadership of cross-functional teams
Knowledge of Risk Evaluation Mitigation Strategies
Ability to work in a global matrixed environment
Key Requirements
Ph.D. in epidemiology, pharmacoepidemiology, public health, pharmacy, or relevant scientific field
7 years of relevant experience in pharmacoepidemiology
Sound methodological training in observational health research
Excellent oral and written communication skills with solid medical writing experience
Proven leadership skills and ability to manage multiple tasks