Syneos Health hiring Medical Writer II in Pune
- About Syneos Health
- Key Job Responsibilities
- Writing & Documentation:
- Regulatory Compliance:
- Review & Mentorship:
- Project Support:
- Budget & Timeline:
- Eligibility Criteria
- Educational Qualifications:
- Experience Required:
- Technical & Soft Skills:
- 📍 Job Location
- How to Apply
- Quick Summary Table
Medical Writer II (CTT) – BSc/BA with 3+ Yrs Experience | Syneos Health Pune
Syneos Health hiring Medical Writer II in Pune | Min. BSc/BA with 3+ years in CTD/CTT & regulatory writing | Apply now for a global pharma career!
Syneos Health Hiring: Medical Writer II (CTT) – Pune, India
Are you passionate about transforming clinical data into impactful scientific documents? Syneos Health, a global leader in biopharmaceutical solutions, is inviting applications for the role of Medical Writer II within its Clinical Trial Transparency (CTT) team in Pune. This is an excellent opportunity for professionals with a scientific background and regulatory writing experience to join a pioneering organization that supports 94% of all novel FDA drug approvals.
About Syneos Health
Syneos Health® integrates clinical development and commercialization to accelerate biopharma success globally. With a workforce of over 29,000 professionals across 110 countries, the company partners with top pharma clients to bring life-changing therapies to market faster.
Work Here Matters Everywhere – Join a culture that champions diversity, innovation, and growth.
Key Job Responsibilities
Writing & Documentation:
- Draft, edit, and finalize documents including study protocols, clinical study reports, investigator brochures, and annual reports.
- Interpret complex clinical data into concise, scientifically sound documents.
Regulatory Compliance:
- Adhere to ICH-E3, FDA, and EMA regulatory guidelines.
- Ensure compliance with company SOPs and client templates.
Review & Mentorship:
- Peer-review team submissions for clarity, consistency, and regulatory alignment.
- Provide mentorship to junior writers as needed.
Project Support:
- Coordinate with biostatistics, data management, regulatory affairs, and medical teams.
- Conduct online literature reviews as necessary.
Budget & Timeline:
- Work within assigned project timelines and budget hours.
- Keep pace with evolving client expectations and medical writing trends.
Eligibility Criteria
Educational Qualifications:
- Bachelor of Science (BSc) or Bachelor of Arts (B.A.) in English, Communications, Social Sciences with medical/scientific writing exposure.
Courses that meet eligibility:
- BSc. in Life Sciences, Biotechnology, Clinical Research, Microbiology, Biochemistry
- B.A. in English, Journalism, or Technical Writing with science understanding
Experience Required:
- Minimum 3 years of hands-on experience in CTD, CTT, and regulatory medical writing.
- Experience with ClinicalTrials.gov, EudraCT, or other global trial registries is highly preferred.
Technical & Soft Skills:
- Advanced knowledge of Microsoft Word, Excel, and PowerPoint
- Strong command of English grammar, AMA style guide, and data interpretation
- Excellent teamwork and independent problem-solving skills
📍 Job Location
Pune, India
Remote flexibility: May require less than 25% travel
How to Apply
Apply directly through the official Syneos Health careers portal: 👉 Apply Here
Quick Summary Table
| Company Name | Current Vacancies in Departments |
|---|---|
| Syneos Health | Clinical Trial Transparency (Medical Writing) |
| Required Education | Experience Required |
| BSc. Life Sciences, B.A. English/Communications | Min. 3 years in CTD/CTT, regulatory writing |
To apply for this job please visit www.syneoshealth.com.
