Associate Director, Real-World Evidence Studies

rview: 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 Referrals increase your chances of interviewing at Meet Life Sciences by 2x Inferred from the description for this job Medical insurance Vision insurance 401(k) Get notified about new Director of Studies jobs in San Rafael, CA . #J-18808-Ljbffr