Associate Director, Real-World Evidence Studies

Meet Life Sciences; San Rafael (CA); Hybrid; USD 90,000 - 150,000; Full time

Benefits offered by this job

Medical insurance

Vision insurance

401(k)

Job summary

Join a forward-thinking company as a Real World Evidence Lead, where you will support the design and execution of impactful RWE studies. This role is pivotal in informing product strategy and enhancing the understanding of diseases and treatment outcomes. Collaborate with a global medical affairs team and leverage your expertise in epidemiological analysis and strategic study execution. If you are passionate about making a difference in the pharmaceutical industry and have a strong background in epidemiology, this is the perfect opportunity for you to shine in a dynamic and collaborative environment.

Qualifications

• 2+ years of epidemiologic research in pharma/biotech.
• Experience with real world data and medical terminologies.

Responsibilities

• Design and implement RWE studies aligned with product evidence plans.
• Lead secondary data analysis using EHR, claims, and registry data.

Skills

Epidemiological research

Statistical programming (SAS, Python, R)

Project management

Communication skills

Cross-functional collaboration

Education

Doctorate in Epidemiology

Master's in Public Health

Tools

EHR data

Claims data

Registry data

HL7 standards

FHIR standards

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:

1. Design and implement RWE studies aligned with product evidence plans
2. Develop protocols, conduct literature reviews, and analyze disease understanding and treatment patterns
3. Support post-marketing safety/effectiveness studies and registries
4. Lead secondary data analysis using EHR, claims, and registry data
5. Collaborate with internal and external research partners and oversee study execution
6. Prepare regulatory documents and support commercial forecasting

Qualifications:

1. Doctorate or Master's degree in Epidemiology, Public Health, or related discipline
2. 2+ years (PhD) or 5+ years (Master’s) of epidemiologic research in pharma/biotech
3. Experience with real world data (EHR, claims, registries), data standards (e.g., HL7, FHIR), and medical terminologies (e.g., ICD-10)
4. Proficiency in statistical programming (SAS, Python, or R)
5. Strong project management, communication, and cross-functional collaboration skills
6. 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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