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Syneos Health

Senior Research Associate

Syneos Health

Research Associate/Senior Research Associate focused on real-world evidence research initiatives at Syneos Health. Collaborating on study design, data analysis, and reporting with teams across the globe.

Posted 6/30/2026full-timeArizona, Maine, Ohio, Rhode Island • 🇺🇸 United StatesSeniorWebsite

About the role

Key responsibilities & impact
  • Contribute to study design and methodology development
  • Develop innovative approaches, frameworks and solutions to client problems
  • Deliver project outputs that meet established quality standards, timelines, and budget requirements
  • Conduct structured literature reviews and targeted secondary research to support RWE initiatives
  • Participate in qualitative research activities, including patient interviews, to generate actionable healthcare insights
  • Analyze and interpret qualitative and quantitative ‘real-world’ data for deliverables
  • Conduct workshops and moderate discussions
  • Present results to external clients
  • Contribute to the development of: Study protocols, Technical reports, Manuscripts and scientific posters, Client presentations
  • Develop and format materials using PowerPoint, Word, and Excel
  • Summarize and synthesize complex clinical and outcomes data into clear, structured findings
  • Support retrospective and prospective real-world studies under senior guidance
  • Demonstrate openness to leveraging emerging technologies, including AI-enabled tools, to improve efficiency, analytical rigor, and personal productivity

Requirements

What you’ll need
  • Master’s degree in public health, epidemiology, health sciences, or a related field (or equivalent combination of education and experience)
  • 1–2 years (Research Associate), or 2+ years (Senior Research Associate) of relevant experience within the life sciences industry (e.g., HEOR, RWE, clinical research, pharmaceutical industry, healthcare consulting, or academia)
  • Foundational understanding of real-world research methodologies and study design
  • Overall understanding of the drug development lifecycle
  • Strong analytical and critical thinking skills
  • Proficiency in Microsoft Excel, Word, and PowerPoint
  • Working knowledge of statistical software (e.g., SAS, R, Stata, or similar)
  • Business-level conversational English (written and spoken)

Benefits

Comp & perks
  • 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
  • Committed to building an inclusive culture

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools
Real-World Research MethodologiesStudy DesignData AnalysisQualitative ResearchLiterature ReviewStatistical AnalysisProject ManagementClinical ResearchHealthcare InsightsData Synthesis
Soft Skills
Critical ThinkingCommunicationCollaborationModerationPresentation Skills