Location: Remote, candidates must be US-based.
Responsibilities:
- Design and conduct epidemiological studies to generate real-world evidence within time, budget, and quality standards, including but not limited to: natural history of disease, population characterization, assessment of treatment patterns and unmet need, development of external comparators, benchmarking of clinical outcomes, comparative safety and effectiveness research, and post-authorization studies.
- Lead the development of study protocols, analysis plans, and study reports to address methodologic questions relevant to RWE.
- Identify suitable data sources for the timely execution of the RWE strategy.
- Construct cohorts using RWD sources (e.g., claims, EHR) and evaluate key variables, including diagnosis and procedures codes; plan validation studies as needed.
- Conduct analyses for descriptive and comparative research questions using RWD.
- Assist in communicating observational research results and methods, including developing sections of regulatory documents, reports, publications, and white papers.
- Support effective communication of study/analysis results to aid internal and external decision-making.
- Contribute to developing processes and training to enhance the efficiency, quality, and impact of activities.
- Coauthor abstracts and manuscripts for external dissemination of methodologic study findings.
Requirements:
- PhD in Epidemiology or related field with at least four (4) years of relevant post-doctoral experience; a Master’s degree with 7-9 years of experience may be acceptable.
- Experience in oncology, especially solid cancers such as breast cancer, is preferred.
- Deep understanding of observational research methods, including designing studies, protocols, statistical analysis plans, and reports.
- Extensive knowledge of secondary data sources and experience with secondary data analysis, including electronic medical records and claims databases.
- Proven record of scientific publications demonstrating expertise in observational study design, analysis, and interpretation is preferred.
- Ability to work independently and develop productive cross-functional collaborations in a matrix environment.
- Strong skills in managing priorities and performance targets.
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
IQVIA is an equal opportunity employer. All qualified applicants will receive consideration without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other legally protected status. More info at https://jobs.iqvia.com/eoe
The base pay range for this role is $110,500 - $276,100 annually, with actual offers based on qualifications, location, and other factors. Additional incentives, bonuses, and benefits may be provided.
At IQVIA, we value diverse talent with curious minds and a commitment to innovation and impact. Everyone contributes to our goal of improving lives worldwide. Thank you for your interest in growing your career with us.
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