
10,000+ employees
🧬 Biotechnology
💊 Pharmaceuticals
⚕️ Healthcare Insurance
Biotechnology • Pharmaceuticals • Healthcare Insurance
Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. They translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities. By utilizing advanced technologies and insights, Syneos Health collaborates with clients to speed the delivery of important therapies to patients worldwide, offering services that span the entire clinical-to-commercial spectrum.
🕒 April 30
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10,000+ employees
🧬 Biotechnology
💊 Pharmaceuticals
⚕️ Healthcare Insurance
Biotechnology • Pharmaceuticals • Healthcare Insurance
Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. They translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities. By utilizing advanced technologies and insights, Syneos Health collaborates with clients to speed the delivery of important therapies to patients worldwide, offering services that span the entire clinical-to-commercial spectrum.
• Responsible for executing a variety of claims database analyses, prospective and retrospective multi-site observational studies, and patient reported outcomes studies, producing high quality RWE research and raising awareness of RWE. • A significant portion of this role is dedicated to medical writing, supporting the design and execution of Real World Evidence (RWE) studies. • The individual will contribute to the development of study protocols across a range of methodologies, including global and regional healthcare claims database studies, multi-site observational studies, Patient-Reported Outcomes (PRO) studies, and systematic literature reviews. • This role requires close collaboration with cross-functional teams to ensure scientific rigor, clarity of research objectives, and high-quality, client-ready deliverables. • Responsible for delivery of project outputs that are within budget and timelines and meet quality standards. • With oversight, prepare draft study reports and external publications. • Contribute to the development of materials for congress presentations and manuscripts. • Primary sponsor contact for assigned projects. • Participate in business development activities.
• Advanced degree (Master’s) in epidemiology, economics, public health or other health related fields or acceptable equivalent combination of education and experience. • At least two years’ experience writing protocols, study reports, and similar documents for RWE/RWLP work. • The ability to develop understanding of retrospective and prospective research methods, phase IIIB/IV study designs, HEOR and related methodology. • Strong personal communication and good teamwork skills. • Candidate must demonstrate regional Real World Research experience. • Other experience includes extensive experience with personal computers; knowledge of statistical software. • Fluent in written English. • Regional language fluency is preferred (Japanese, Chinese, Korean).
• 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. • We are committed to building an inclusive culture – where you can authentically be yourself.
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