Medical Writer – Clinical Trial Transparency Job At Syneos Health
The Medical Writer II (Clinical Trial Transparency) role at Syneos Health offers an exciting opportunity to support clinical trial disclosure, protocol writing, and medical communication. This Medical Writer Job position empowers professionals to contribute to global clinical research by ensuring the delivery of accurate, compliant, and high-quality medical writing deliverables. Graduates seeking Pharmacy Jobs and want to kick-start their career in Pharmacy careers can apply now.
Job Details
- Job Title: Medical Writer II – Clinical Trial Transparency
- Location: Pune, Maharashtra, India
About the Company
Syneos Health® is a leading integrated biopharmaceutical solutions organization committed to accelerating clinical and commercial outcomes. With a focus on patient-centric innovation, the company operates in over 110 countries, collaborating across disciplines to streamline drug development, clinical trial transparency, and medical communications while fostering an inclusive and supportive workplace.
Educational Requirements for a Medical Writer Job
- Bachelor’s degree in a pharma discipline; graduate degree preferred
- Strong understanding of clinical research principles and medical terminology
Key Responsibilities for a Medical Writer Job
- Develop, write, and edit clinical trial documents such as study protocols, reports, patient narratives, and investigator brochures
- Ensure compliance with regulatory standards (FDA, ICH-E3, GPP) and company SOPs
- Review statistical analysis plans, table/figure/listing specifications for content and consistency
- Perform clinical literature searches and support protocol registration
- Mentor junior medical writers and serve as a peer reviewer
- Collaborate with data management, biostatistics, regulatory affairs, and medical affairs teams
- Manage project timelines, budgets, and administrative tasks effectively
Skills Required for a Medical Writer Job
- Knowledge of clinical trial disclosure and registry databases (CT.gov, CTIS, EUDRACT, Pharma CM/Disclose)
- Strong writing, proofreading, and presentation skills
- Understanding of FDA, ICH regulations, and good publication practices
- Proficiency in MS Office and medical writing software
- Strong project and time management skills
- Excellent interpersonal and collaborative abilities
Why This Job Role?
This role allows professionals to contribute to the integrity and transparency of global clinical trials while gaining experience across regulatory submissions, medical communications, and protocol development. It offers exposure to cutting-edge clinical research processes and collaboration with a global team at a leading biopharmaceutical organization. Graduates seeking Pharmacy Jobs and want to kick-start their career in Pharmacy careers can apply now.
