RWE Senior Epidemiologist​/Senior Observational Research Scientist

RWE Senior Epidemiologist/Senior Observational Research Scientist

Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. Our Clinical Development model puts the customer and the patient at the center of everything we do.

We are continuously looking for ways to simplify and streamline our work to make Syneos Health easier to work with and easier to work for.

• We are passionate about developing our people through career development and progression, supportive line management, technical and therapeutic area training, peer recognition, and a total rewards program.
• We are committed to our Total Self culture, where you can authentically be yourself.
• We are continuously building the company we want to work for and our customers want to work with, fostering diversity of thought, background, culture, and perspective.

• 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.
• Plan, design, and conduct analyses for internal and external decision‑making (e.g., regulatory responses, rapid safety queries).
• Lead the identification of fit‑for‑purpose data for the timely execution of the RWE strategy.
• Construct cohorts using RWD sources (claims, EHR), evaluate key variables, and plan validation studies as needed.
• Contribute to communication of observational research results and methods, including sections of regulatory documents, reports, publications, and white papers.
• Support 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.
• Technical Expertise
  • Observational research methods (primary and secondary), deep knowledge of biostatistics, analysis methods, and regulatory processes.
  • Ability to design studies independently and translate research questions into study design.
• Subject Matter Expertise
  • Conduct analyses for descriptive and comparative research using RWD (claims, EHR, PRO/COA, registry data) for methodological research questions.

• PhD in Epidemiology, Biostatistics, Psychometrics, or related field with a minimum of four (4) years of post‑doctoral experience, preferably in pharmaceutical industry, biotechnology, or consulting. A master’s degree plus 7‑9 years of experience may be acceptable.
• Deep understanding of observational research methods and experience supporting design and conduct of observational research.
• Extensive knowledge of secondary data sources and experience with secondary data analysis (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 increasing autonomy and develop productive cross‑functional collaborations in a matrix environment.
• Ability to manage priorities and performance targets.
• Experience leading drug development projects for 2+ years for the therapeutic area of assignment preferred.

• Company car or car allowance.
• Health benefits including medical, dental, and vision.
• Company match 401(k).
• Eligibility to participate in an Employee Stock Purchase Plan.
• Eligibility to earn commissions/bonus based on company and individual performance.
• Flexible paid time off (PTO) and sick time (subject to state and local regulations).

Tasks, duties, and responsibilities are not exhaustive. The Company may assign other tasks or duties at its discretion. Equivalent experience or education may be considered. The Company complies with all relevant legislation, including the EU Equality Directive and the Americans with Disabilities Act.