[Hiring] Senior Epidemiologist, Oncology, Breast Cancer, Real World Evidence - FSP @IQVIA

This description is a summary of our understanding of the job description. Click on 'Apply' button to find out more. 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. Apply tot his job