
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.
Every day we perform better because of how we work together, as one team, each the best at what we do. We bring a wide range of talented experts together across a wide range of business-critical services that support our business. Every role within Corporate is vital to furthering our vision of Shortening the Distance from Lab to Life®.
Discover what our 29,000 employees, across 110 countries already know.
WORK HERE MATTERS EVERYWHERE
Why Syneos Health
Job Responsibilities
Job Summary
As part of the company’s strategic research and Business Insights function, the Research Associate role provides intelligence support to internal teams, customers, and stakeholders across client billable projects, business development initiatives, strategic account planning, competitive intelligence reporting, and Thought Leadership publications. Applies drug development knowledge, particularly the clinical trial process, regulatory pathways, and commercialisation strategy, to synthesise complex secondary research into structured, decision-ready insights. Translates scientific, clinical, and financial information into clear business implications that support revenue growth and strategic positioning for Syneos Health.
Core Responsibilities
• Conduct structured secondary research using subscribed intelligence platforms, regulatory databases, clinical trial registries, investor communications, financial disclosures, and publicly available data sources.
• Synthesise multi-source data into executive-ready outputs including competitive intelligence briefs, earnings analyses, strategic account summaries, pipeline tracking reports, and landscape assessments.
• Support proposal development and bid defences with high-precision, rapid-turnaround research.
• Interpret clinical development data including phase progression, endpoints, regulatory pathways, and modality differentiation.
• Identify strategic inflection points such as funding events, portfolio reprioritisation, partnership activity, workforce shifts, and geographic expansion.
• Leverage AI-enabled research tools responsibly while maintaining rigorous validation standards.
• Contribute to internal knowledge systems, workflow optimisation, and research automation initiatives.
• Collaborate across teams while managing multiple concurrent priorities in a deadline-driven environment.
Qualifications
Education: Bachelor’s degree in life sciences, healthcare, pharmacy, biotechnology, or related scientific field required. Advanced degree preferred.
Experience: 1–3 years of experience within CRO, pharmaceutical, biotech, consulting, or strategic research environment preferred.Additional Qualifications
• Strong analytical and problem-solving skills with ability to synthesise complex information into structured deliverables.
• Foundational understanding of drug development lifecycle and regulatory frameworks.
• Experience within therapeutic areas or specialised healthcare functions preferred.
• Ability to translate scientific information into commercially relevant insights.
• Experience leveraging AI-enabled research tools and supporting knowledge automation welcomed.
• Exposure to building or supporting internal knowledge agents welcomed.
• Fluency in additional languages considered an advantage.
• Strong Microsoft Office skills.
Critical Skills
• Structured analytical thinking
• Clinical and pipeline interpretation
• Competitive intelligence development
• Scientific-to-commercial translation
• Executive-level written communication
• AI-assisted research validation
• Time management under pressure
• Cross-functional collaboration
Disclaimer
Tasks, duties, and responsibilities as listed are not exhaustive. The Company may assign other responsibilities as required. Equivalent experience and education may be considered. Nothing herein creates an employment contract. The Company complies with all applicable employment legislation and equal opportunity standards.
Get to know Syneos Health
Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.
No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.
Additional Information
Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.