Epidemiologist, Inflammation, Real World Evidence (FSP Sponsor Dedicated)

IQVIA • San Francisco, CA

1d • $109,200 - $273,000 • Remote

About The Position

IQVIA is hiring an Epidemiologist to support a sponsor-dedicated inflammation program. The role independently executes real-world evidence work supporting early clinical development, using epidemiologic methods and real-world data to characterize disease natural history and landscapes, assess study feasibility, and contribute to Phase 1–3 development programs. It is a hands-on execution position focused on producing high-quality protocols, clinical study reports, and related scientific deliverables with a high degree of independence. The position is home-based in the United States, with a West Coast location preferred. The employee will work closely with one sponsor while drawing on IQVIA's global expertise and scientific community.

Requirements

• PhD in Epidemiology.
• Demonstrated experience applying epidemiology and real-world evidence to Phase 1–3 clinical development programs.
• Prior pharmaceutical industry experience.
• Knowledge of regulatory-grade real-world evidence expectations and rigorous observational research methods.
• Epidemiology experience in inflammation or a closely related therapeutic area.
• Experience conducting natural history, disease landscape, and study feasibility work using real-world data.
• Experience developing study protocols, clinical study reports, and related epidemiology deliverables.
• Ability to work independently, take ownership of assigned work, and execute with limited supervision.
• Strong scientific writing, analytical, project management, and stakeholder communication skills.

Responsibilities

• Independently execute epidemiology and real-world evidence activities supporting inflammation programs in early clinical development, including Phases 1–3.
• Use real-world data and epidemiologic methods to describe disease natural history and characterize inflammation disease landscapes.
• Conduct feasibility assessments of research questions, available data, study populations, endpoints, and potential study approaches.
• Develop and contribute to study protocols, analysis plans, study reports, clinical study reports, and other scientific deliverables.
• Support regulatory-grade real-world evidence studies using sound epidemiologic methods and appropriate documentation standards.
• Translate assigned research objectives into clear, accurate, and timely deliverables through hands-on study execution.
• Interpret study findings and communicate methods, assumptions, limitations, and results to sponsor stakeholders and cross-functional partners.
• Proactively manage assigned work and resolve execution issues with limited supervision or day-to-day direction.
• Collaborate with sponsor teams across functions and time zones in a sponsor-dedicated model.

Benefits

• Access to IQVIA's global network and scientific community to support continued growth.
• Health and welfare benefits may be offered, depending on the position.
• Incentive plans, bonuses, and/or other forms of compensation may be offered, depending on the position.

What This Job Offers

• Job Type: Full-time
• Career Level: Senior
• Education Level: Ph.D. or professional degree