Perform feasibility analysis for studies ·
Conduct literature review ·
Plan observational studies and draft protocol synopsis (or protocol concept sheet) ·
Determine observational study design criteria – including source data, analytical methods and analysis plans ·
Draft and review observational study protocols ·
Draft and review observational study analysis specifications, including statistical analysis plans (SAPs) ·
Draft and review observational study reports · Conduct observational studies, both primary data collection and secondary data use studies · Conduct study data analysis according to observational methods ·
Conduct data analysis according to observational methods ·
Review analysis outputs for quality, including study analysis, ad hoc analysis, analysis to support conference or publications ·
Conduct quality review of all deliverables to ensure data and results are accurate ·
Work with scientific and operational stakeholders to identify and resolve issues ·
Collaborate with study teams, vendors and other stakeholders to advance study and analysis deliverables ·
Work with relevant stakeholders to meet study milestones and timelines ·
Participate in program or study planning meetings ·
Actively adapt and adjust priorities to ensure timely and quality completion of assigned tasks ·
Contribute to ongoing improvement of programming processes and methodology ·
Perform other related duties as required by the Department.
Graduate degree in Epidemiology ·
7 – 10+ years industry experience as an epidemiologist ·
Oncology RWD/RWE Study Experience preferred
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