Director, Epidemiology RWE – Onco or Immunology
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Job Description
Director of Epidemiology RWE at Syneos Health focusing on Onco or Immunology. Leading study protocol development and managing epidemiological projects to enhance healthcare outcomes.
Responsibilities:
- 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 (e.g., responses to regulatory authorities, rapid analyses of safety queries)
- Lead the identification of fit-for-purpose data for the timely execution of the RWE strategy
- Constructed cohorts using RWD sources (e.g., claims, EHR) and evaluate key variables, including diagnosis and procedures codes, and plan validation studies as needed
- Contribute to the communication of observational research results and methods, including development of pertinent sections of regulatory documents, reports, publications, white papers
- 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
Requirements:
- PhD in Epidemiology, Biostatistics, Psychometrics, or related field with a minimum of four (4) years of relevant post-doctoral experience, preferably in pharmaceutical industry, biotechnology, or consulting environment
- Deep understanding of observational research methods and experience to support the design and conduct of observational research, including protocol, statistical analysis plan, and study report development
- Extensive knowledge of secondary data sources and experience with secondary data analysis, including electronic medical record 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 an increasing level of autonomy and to develop productive cross-functional collaborations in a matrix environment
- Ability to manage priorities and performance targets
- Experience in leading drug development project for 2+ years for therapeutic area of assignment preferred
Benefits:
- Health benefits to include Medical, Dental and Vision
- Company match 401k
- Eligibility to participate in Employee Stock Purchase Plan
- Eligibility to earn commissions/bonus based on company and individual performance
- Flexible paid time off (PTO) and sick time
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