Senior Research Associate

Syneos Health

Real-world evidence researcher supporting retrospective and prospective studies for life sciences clients. Developing clinical, outcomes, and market-access insights across the drug development lifecycle.

Posted 8/12/2026full-timeArizona, Maine, Ohio, Rhode Island • 🇨🇦 Canada, 🇺🇸 United StatesSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in real-world research methodologies and study design, with strong analytical skills and proficiency in statistical software. Capable of delivering high-quality project outputs while effectively communicating results to clients and collaborating within teams.

Highest-signal resume keywords

Master’s Degree In Public HealthReal-World Research MethodologiesStatistical Software ProficiencyAnalytical And Critical Thinking SkillsMicrosoft Office Suite

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Study DesignData AnalysisQualitative ResearchQuantitative ResearchLiterature ReviewProject ManagementStatistical AnalysisData InterpretationClient PresentationsTechnical Report Writing

Soft Skills

Clear CommunicationTeam CollaborationAttention To DetailTime ManagementIntellectual Curiosity

Tools & Technologies

Microsoft ExcelMicrosoft WordMicrosoft PowerPointSASRStataAI-Enabled Tools

Industry Keywords

Drug Development LifecyclePublic HealthEpidemiologyHealth SciencesClinical Data

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 meeting quality standards, timelines, and budget requirements
Conduct structured literature reviews and targeted secondary research
Participate in qualitative research activities, including patient interviews
Analyze and interpret qualitative and quantitative real-world data
Conduct workshops and moderate discussions
Present results to external clients
Contribute to study protocols, technical reports, manuscripts, scientific posters, and client presentations
Develop and format materials using PowerPoint, Word, and Excel
Summarize and synthesize complex clinical and outcomes data
Support retrospective and prospective real-world studies under senior guidance
Leverage emerging technologies, including AI-enabled tools, to improve efficiency and analytical rigor

Requirements

What you’ll need

Required Master’s degree in public health, epidemiology, health sciences, or a related field, or equivalent combination of education and experience
1–2 years of relevant experience for Research Associate, or 2+ years for Senior Research Associate
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 such as SAS, R, Stata, or similar
Business-level conversational English, written and spoken
Academic or industry research experience preferred
Experience conducting analyses in databases and/or registries preferred
Clear and professional communication skills
Strong teamwork and collaboration
Attention to detail and commitment to quality
Ability to manage multiple priorities in a structured, deadline-driven environment
Intellectual curiosity and commitment to continuous improvement
Willingness to travel approximately 10%

Benefits

Comp & perks

Career development and progression
Supportive and engaged line management
Technical and therapeutic area training
Peer recognition and total rewards program
Inclusive culture
Access to experienced mentors
Structured development opportunities
Flexible hybrid work model
Comprehensive resources including emerging technologies, data, science and knowledge sharing
Approximately 10% travel opportunity