FSP Epidemiologist (Oncology)

About the position The FSP Epidemiologist (Oncology) will design and conduct epidemiological studies to generate real-world evidence within time, budget, and quality standards. Responsibilities include studying the natural history of disease, population characterization, assessment of treatment patterns and unmet needs, development of external comparators, benchmarking of clinical outcomes, comparative safety and effectiveness research, and post-authorization studies. The role also involves supporting the development of study protocols, analysis plans, and study reports to address methodologic questions of priority to Real World Evidence (RWE). Additionally, the epidemiologist will identify fit-for-purpose data for timely execution of the RWE strategy, construct cohorts using Real World Data (RWD) sources, and conduct analyses for descriptive and comparative research. The position requires effective communication of research results and methods, contributing to regulatory documents, reports, publications, and white papers, as well as coauthoring abstracts and manuscripts for external dissemination. Responsibilities • Design and conduct epidemiological studies to generate real-world evidence. • Support development of study protocols, analysis plans, and study reports. • Identify fit-for-purpose data for timely execution of the RWE strategy. • Construct cohorts using RWD sources and evaluate key variables. • Conduct analyses for descriptive and comparative research using RWD. • Contribute to the communication of observational research results and methods. • Support effective communication of study/analysis results. • Contribute to the development of processes and training for efficiency and quality. • Coauthor abstracts and manuscripts for external dissemination. Requirements • PhD in Epidemiology or related field with a minimum of two years of relevant post-doctoral experience, preferably in pharmaceutical industry, biotechnology, or consulting environment. • Master's degree in epidemiology or relevant scientific field, plus five years of experience in lieu of PhD may be acceptable. • Experience in oncology research, specifically in solid tumors. • Understanding of observational research methods and experience in designing and conducting observational research. • Knowledge of secondary data sources and experience with secondary data analysis, including electronic medical records and/or medical claims databases. • A record of scientific publications demonstrating expertise in observational study design, analysis, and interpretation is preferred. • Demonstrated ability to function with increasing autonomy and develop productive cross-functional collaborations. • Ability to manage priorities and performance targets. Nice-to-haves • Experience in the pharmaceutical industry or consulting environment. • Strong publication record in observational research. Benefits • Health and welfare benefits. • Incentive plans and bonuses. Apply tot his job