Job Description
Role Description
- Join IQVIA’s Sponsor-Dedicated FSP team and help advance healthcare through real-world evidence. In this role, you’ll work closely with one sponsor, gaining deep knowledge of their therapies while leveraging IQVIA’s global expertise.
- Design and conduct epidemiological studies to generate real-world evidence within time, budget, and quality standards.
- Lead development of study protocols, analysis plans, and study reports to answer research questions of priority to RWE.
- Lead, design, and manage epidemiological, biomarker and/or data science projects.
- Lead, plan, design, and conduct analyses for internal and external decision making.
- Lead the identification of fit-for-purpose data for the timely execution of the RWE strategy.
- Construct cohorts using RWD sources and evaluate key variables.
- Contribute to the communication of observational research results and methods.
- Support the effective communication of study/analysis results to support internal and external decisions.
- Coauthor abstracts and manuscripts for external dissemination of methodologic study results.
- Contribute to the development of processes and training aimed at increasing the efficiency, quality, and impact of functional activities.
- Qualifications
- PhD in Epidemiology with a minimum of four (4) years of post-doctoral experience, preferably at a pharmaceutical company.
- Master’s degree in Epidemiology plus 7-9 years of experience in lieu of PhD may be acceptable.
- Oncology Specific: expert knowledge and extensive experience with cancer epidemiology.
- Pharmaco Epidemiology Specific: expert knowledge and extensive experience with pharmacoepi methods.
- Deep understanding of observational research methods.
- Extensive knowledge of secondary data sources and experience with secondary data analysis.
- A record of scientific publications demonstrating expertise in observational study design, analysis, and interpretation is preferred.
- Demonstrated ability to function with an increasing level of autonomy.
- Ability to manage priorities and performance targets.
- Requirements
- Ability to design studies independently.
- Extensive experience with oncology EMR databases.
- Extensive experience with conducting cancer epidemiology studies.
- Expert understanding of regulatory requirements for safety reporting and analysis.
- 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.
- This is your chance to make an impact, while building a career that matters.
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