Senior Epidemiologist, Immunology, RWE (FSP Sponsor Dedicated)
About the role
This role supports the Inflammation, Real World Evidence team at IQVIA, providing scientific and strategic epidemiology support for clinical development and drug safety activities. The Senior Epidemiologist will design and conduct observational research studies, assess evidence gaps, evaluate safety profiles, and develop evidence strategies to support regulatory interactions and clinical development programs.
Responsibilities
- Design and conduct observational research studies
- Assess evidence gaps
- Evaluate safety profiles
- Develop evidence strategies to support regulatory interactions and clinical development programs
- Collaborate with cross-functional teams including Clinical Development, Safety, Regulatory Affairs, Biostatistics, and Real-World Evidence stakeholders
Requirements
- 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
Qualifications
- 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
Benefits
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. Access IQVIA’s global network who supports your growth.
Pay
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).
Schedule
This is a fully remote position based in the United States.