Job Description:

• Description · 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.
• Experience · Graduate degree in Epidemiology · 7 – 10)+ years industry experience as an epidemiologist · Oncology RWD/RWE Study Experience preferred