Director, Epidemiology RWE – Onco or Immunology

Syneos Health

Director of Epidemiology RWE at Syneos Health focusing on Onco or Immunology. Leading study protocol development and managing epidemiological projects to enhance healthcare outcomes.

Posted 7/14/2026full-timeRemote • Connecticut, District of Columbia, Maryland, New Hampshire, Virginia • 🇺🇸 United StatesLead💰 $118,700 - $207,800 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in leading the design and execution of observational research projects, including protocol and statistical analysis plan development, while effectively communicating results to support decision-making. Possesses extensive knowledge of secondary data sources and a strong publication record in observational study design and analysis.

Highest-signal resume keywords

PhD In EpidemiologyObservational Research MethodsSecondary Data AnalysisDrug Development Project ManagementScientific Publication Record

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Study Protocol DevelopmentStatistical Analysis Plan DevelopmentCohort Construction Using RWDData Science Project ManagementEpidemiological Analysis

Soft Skills

Cross-Functional CollaborationAutonomyPriority Management

Tools & Technologies

Electronic Medical Record DatabasesMedical Claims Databases

Industry Keywords

Real World EvidencePharmaceutical IndustryBiotechnologyConsulting Environment

About the role

Key responsibilities & impact

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

What you’ll need

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

Comp & perks

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