Associate Director RWE & Epidemiology
Listed on 2026-02-19
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Research/Development
Data Scientist, Research Scientist
Associate Director, Real-World Evidence (RWE Scientist)
Location:
Eastern United States (onsite/hybrid initially until onboarding completion)
Engagement: 7-months minimum
About the Role
We are supporting our client in the search for a highly experienced Real‑World Evidence (RWE) Scientist at Associate Director level. This senior, hands‑on position provides temporary coverage for ongoing Phase IV and post‑approval RWE studies. The role involves leading real‑world research, managing vendors, and driving EU‑facing evidence planning within a global Medical Affairs organisation. This is an individual contributor role requiring strong scientific judgment and the ability to work autonomously.
Key Responsibilities
- Lead the design, execution, and analysis of real‑world and observational research studies with methodological rigour
- Manage in‑flight Phase IV and post‑approval epidemiologic studies and oversee CRO/vendor performance
- Lead RWE feasibility assessments and contribute to evidence planning, including activities focused on Europe.
- Develop protocols for real‑world studies and pragmatic trials; provide methodological and scientific guidance
- Support evidence reviews, strategic decision‑making, and communication with internal stakeholders.
- Support internal and external scientific communication (readouts, abstracts, posters, manuscripts).
- May contribute to systematic literature reviews (SLRs) and meta‑analyses as required.
Requirements
- Advanced degree: MD, PhD, or MS in Epidemiology, Biostatistics, Public Health, or related field.
- 8–10 years of progressive epidemiology or RWE experience, including at least 5 years in Pharma/Biotech.
Demonstrated experience leading:
- Prospective/Phase IV epidemiologic studies
- Retrospective real‑world data analyses (claims/EHR)
- Proficiency with SAS, R, Stata and deep understanding of RWD structures.
- Ability to step in quickly, work independently, and take ownership with minimal ramp‑up.
- Flexibility for cross‑timezone collaboration (EU and Australia).
Preferred
- Experience supporting regulatory/HTA‑facing RWE deliverables and post‑approval commitments
- Background in vaccines or infectious disease.
- Strong R programming skills, including ability to develop or enhance Shiny apps; experience with RWD extraction/cleaning.
- Experience in global Medical Affairs and oversight of vendors/CROs.
How to Apply
If you are interested in this opportunity, please apply directly or email:
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