Senior Epidemiologist, Immunology, RWE (FSP Sponsor Dedicated)

Key responsibilities include designing and conducting observational research studies, assessing evidence gaps, evaluating safety profiles, and developing evidence strategies to support regulatory interactions and clinical development programs. The Senior Epidemiologist will collaborate closely with cross-functional teams, including Clinical Development, Safety, Regulatory Affairs, Biostatistics, and Real-World Evidence stakeholders, to ensure appropriate epidemiologic approaches are applied to address critical business and scientific questions.

The ideal candidate will have deep expertise in epidemiologic methods, demonstrated experience working within pharma or biotech, and a thorough understanding of regulatory requirements related to clinical development and safety evidence generation.

- Doctoral degree (PhD, ScD, or equivalent) in Epidemiology.

- 5 to 7 years of epidemiology experience within a pharmaceutical/biotechnology company.

- Demonstrated experience supporting clinical development and/or drug safety.

- Strong expertise in observational research methods and the use of commercial healthcare databases such as HealthVerity, Pharmetrics Plus, TriNetX, or similar real-world data assets.

- Solid understanding of regulatory requirements and evidence needs supporting clinical development, including the generation of evidence to address regulatory questions related to safety profiles and evidence gaps for Phase II and Phase III programs.

- Proven ability to design, execute, and interpret epidemiologic studies that support regulatory, clinical, or safety objectives.

- Experience in Inflammation and Immunology therapeutic areas.

- Knowledge of disease areas such as Atopic Dermatitis, Asthma, Lupus, Immune Thrombocytopenia (ITP), Autoimmune Hemolytic Anemia, or other immune-mediated diseases.

- Experience supporting assets within emerging immunology programs.

- Experience working with primary or hybrid real-world data sources in addition to secondary data sources.

- Prior experience supporting regulatory submissions or interactions with FDA, EMA, or other global health authorities.

- Be part of a forward-thinking team that helps shape the next generation of evidence-based healthcare.

- Work hand-in-hand with one leading sponsor, gaining deep expertise in their therapies.

This is your chance to make an impact, while building a career that matters.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.

Learn more at https://jobs.iqvia.com

The potential base pay range for this role, when annualized, is $109,200.00 - $273,000.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.