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RWE Senior Epidemiologist​/Senior Observational Research Scientist

Job in Morrisville, Wake County, North Carolina, 27560, USA
Listing for: Syneos Health Careers
Full Time position
Listed on 2026-02-21
Job specializations:
  • Research/Development
    Research Scientist, Data Scientist, Clinical Research
  • Healthcare
    Data Scientist, Clinical Research
Salary/Wage Range or Industry Benchmark: 80000 - 100000 USD Yearly USD 80000.00 100000.00 YEAR
Job Description & How to Apply Below

Description

RWE Senior Epidemiologist/Senior Observational Research Scientist

Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.

Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.

Whether you join us in a Functional Service Provider partnership or a Full‑Service environment, you will collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies because we are passionate about changing lives.

Why Syneos Health
  • We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
  • We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture unites us globally, and we dedicate ourselves to taking care of our people.
  • We are continuously building the company we all want to work for and our customers want to work with. By bringing together diverse thoughts, backgrounds, cultures, and perspectives, we create a place where everyone feels they belong.
Job 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.
  • Construct cohorts using RWD sources (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, and white papers.
  • Support the effective communication of study/analysis results to support internal and external decisions.
  • Coauthor abstracts and manuscripts for external dissemination of methodological 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 (both primary and secondary), deep knowledge of biostatistics and analysis methods, understanding of regulatory processes.
    • Ability to design studies independently (i.e., translate research questions to create study design).
  • Subject Matter Expertise
    • Provide subject matter expertise and conduct analyses for descriptive and comparative research using RWD (e.g., claims, EHR, PRO/COA, registry data) for methodological research questions.
Minimum Qualifications
  • PhD in Epidemiology, Biostatistics, Psychometrics, or related field with a minimum of four (4) years of post‑doctoral experience in the pharmaceutical industry, biotechnology, or consulting environment. A master’s degree in epidemiology, biostatistics, bioinformatics, or related field plus 7‑9 years of experience may be acceptable in lieu of a PhD.
  • 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.
  • Record of scientific publications demonstrating expertise in observational study design, analysis, and interpretation is preferred.
  • Demonstrated ability to function with increasing autonomy and to develop productive…
Position Requirements
10+ Years work experience
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