Epidemiologist Jobs

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About The Position

As an Epidemiologist supporting a sponsor-dedicated inflammation program, you will independently execute real-world evidence work that supports early clinical development. You will use epidemiologic methods and real-world data to characterize the natural history of disease, assess disease landscapes, evaluate study feasibility, and contribute to Phase 1–3 development programs. This is a hands-on execution role focused on producing high-quality protocols, clinical study reports, and related scientific deliverables while operating with a high degree of independence. The role is home-based in the United States, with a West Coast location preferred. You will work closely with one sponsor, gaining knowledge of its therapies while drawing on IQVIA’s global expertise. IQVIA describes itself as a global provider of clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

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 clearly communicate methods, assumptions, limitations, and results to sponsor stakeholders and cross-functional partners.
  • Manage assigned work proactively and resolve execution issues with limited supervision or day-to-day direction.
  • Collaborate effectively with sponsor teams across functions and time zones in a sponsor-dedicated model.

Benefits

  • The posting mentions a range of health and welfare benefits, but does not specify individual benefits.

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What This Job Offers

Job Type

Full-time

Career Level

Senior

Education Level

Ph.D. or professional degree

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