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Job description
Associate Director, Real-World Evidence Studies
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Job Title: Real World Evidence Lead (Associate Director)
Location: San Rafael, CA (Hybrid)
Duration: 12-month contract (April 28, 2025 – April 26, 2026)
Schedule: Full-time, 40 hours/week
Overview:
Seeking a Real World Evidence Lead to support the design and execution of real world evidence (RWE) studies as part of a global medical affairs team. This role will contribute to integrated evidence planning, epidemiological analysis, and strategic study execution to inform product strategy and enhance understanding of diseases and treatment outcomes.
Key Responsibilities:
Design and implement RWE studies aligned with product evidence plans
Develop protocols, conduct literature reviews, and analyze disease understanding and treatment patterns
Support post-marketing safety/effectiveness studies and registries
Lead secondary data analysis using EHR, claims, and registry data
Collaborate with internal and external research partners and oversee study execution
Prepare regulatory documents and support commercial forecasting
Qualifications:
Doctorate or Master's degree in Epidemiology, Public Health, or related discipline
2+ years (PhD) or 5+ years (Master’s) of epidemiologic research in pharma/biotech
Experience with real world data (EHR, claims, registries), data standards (e.g., HL7, FHIR), and medical terminologies (e.g., ICD-10)
Proficiency in statistical programming (SAS, Python, or R)
Strong project management, communication, and cross-functional collaboration skills
Rare disease or genetic epidemiology experience a plus
Seniority level
Director
Employment type
Contract
Job function
Research
Industries
Pharmaceutical Manufacturing and Biotechnology Research
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Inferred from the description for this job
Medical insurance
Vision insurance
401(k)
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Worksite address
san rafael, CA, 94911, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.