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About the Role
This role will support the Inflammation, Real World Evidence team, providing scientific and strategic epidemiology support for clinical development and drug safety activities. You will leverage secondary real-world data (RWD) to generate evidence that informs regulatory, safety, and clinical development decisions across the product lifecycle. You will collaborate closely with cross-functional teams to ensure appropriate epidemiologic approaches are applied to address critical business and scientific questions.
Responsibilities
- Designing and conducting observational research studies
- Assessing evidence gaps
- Evaluating safety profiles
- Developing evidence strategies to support regulatory interactions and clinical development programs
- Collaborating closely 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
Skills
- Epidemiology
- Real-world data (RWD)
- Observational research methods
- Commercial healthcare databases
- Regulatory requirements
- Clinical development
- Drug safety
- Inflammation
- Immunology
- Atopic Dermatitis
- Asthma
- Lupus
- Immune Thrombocytopenia (ITP)
- Autoimmune Hemolytic Anemia
- Immune-mediated diseases
- Emerging immunology programs
- Primary real-world data sources
- Hybrid real-world data sources
- Secondary data sources
- Regulatory submissions
- FDA
- EMA
- Global health authorities
Location
- United States
Work Type
- Fully remote
- Full-time
Experience Level
- Senior
Education Level
- Doctoral degree (PhD, ScD, or equivalent) in Epidemiology
Salary/Compensations
- $109,200.00 - $273,000.00
Benefits
- Health and welfare benefits
- Incentive plans
- Bonuses
About the Company
- 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.
- We create connections that accelerate the development and commercialization of innovative medical treatments.
- Everything we do is part of a journey to improve patient outcomes and population health worldwide.
- To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact.
- No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere.
Equal Opportunity
- IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law.
- IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.