Associate Director, Real-World Evidence & Epidemiology
$176,000–$220,000 year
Remote · United States or US
Job Summary
Lead design, protocol development, and execution of prospective observational studies, registries, and retrospective database assessments across early cancer detection programs; translate clinical and market requirements into rigorous study designs; collaborate across Clinical Science, Medical Affairs, Product Management, and Market Access; deliver real-world data assets to support clinical utility metrics and payer coverage strategies; engage external collaborators and contribute to peer-reviewed dissemination; require advanced quantitative training and 7+ years in real-world evidence within life sciences; remote work available in the USA.
Required Qualifications
- Advanced degree (PhD, MPH, MS, PharmD, or equivalent scientific credential) in epidemiology, health outcomes research, biostatistics, or a highly quantitative field
- 7+ years of experience leading real-world evidence generation, observational clinical research, or HEOR portfolios within the life sciences industry
- Documented experience executing observational studies across the entire asset lifecycle, from initial protocol drafting through statistical analysis and publication
- Deep data competency across real-world data sources, including longitudinal medical claims, electronic health records (EHR), and clinical registries
- Direct experience in oncology clinical trials, molecular diagnostics, or early cancer detection programs is preferred
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