Job Description

Director, Epidemiology RWE - Pharma Co Updated: Yesterday. Location: USA-DE-Remote. Job ID: 25108207. We partner with innovators across the drug development and commercialization continuum to accelerate progress. The Clinical Solutions team applies deep expertise to understand and meet customer needs. Job Responsibilities Open to US candidates with no sponsorship needs. Skillset: Senior Epidemiologist – Inflam‑Liver Group, hybrid trial design, CDisc requirements, PharmaCo Epidemiology. Clinical background preferred; PhD required. Lead development of study protocols, analysis plans, and study reports to answer research questions of priority to real‑world evidence. Design and manage epidemiological, biomarker and data science projects. Plan, design and conduct analyses for internal and external decision‑making (e.g., regulatory responses, safety queries). Identify fit‑for‑purpose data for RWE strategy execution. Construct cohorts from RWD sources (claims, EHR), evaluate key variables, and design validation studies as needed. Communicate observational research results and methods, including development of regulatory documents, reports, publications, white papers. Coauthor abstracts and manuscripts for external dissemination. Support effective communication of study/analysis results to inform decisions. Contribute to development of processes and training to enhance efficiency, quality, and impact. Technical Expertise Observational research methods (primary and secondary), deep knowledge of biostatistics, analysis methods, and regulatory processes. Ability to design studies independently, translating research questions into study design. Subject Matter Expertise Provide expertise and conduct analyses for descriptive and comparative research using RWD (claims, EHR, PRO/COA, registry data). Minimum Qualifications PhD in Epidemiology, Biostatistics, Psychometrics, or related field with at least four (4) years of post‑doctoral experience, preferably in pharma, biotech, or consulting. Or Master’s degree with 7–9 years of experience in lieu of a PhD. Deep understanding of observational research methods and experience supporting design, conduct, and reporting of observational studies. Extensive knowledge of secondary data sources and secondary data analysis (electronic medical records, medical claims databases). Record of scientific publications demonstrating expertise in observational study design, analysis, and interpretation (preferred). Demonstrated ability to work autonomously and collaborate productively in a matrix environment. Strong priority and performance management skills. Experience leading drug development projects for two or more years in the therapeutic area of assignment (preferred). Benefits Company car or car allowance. Health benefits (medical, dental, vision). Company match 401(k). 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. Salary Range: $118,700.00 – $207,800.00. Syneos Health is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to any protected characteristic. #J-18808-Ljbffr

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