Syneos Health® is a leading fully integrated biopharmaceutical solutions organization dedicated to accelerating customer success. With a global presence across 110 countries and a team of 29,000 employees, Syneos Health combines clinical, medical affairs, and commercial expertise to deliver impactful healthcare solutions.
The company has contributed to 94% of all Novel FDA Approved Drugs over the past five years, along with 95% of EMA Authorized Products, demonstrating its leadership in clinical research and drug development.
Why Join Syneos Health?
- Career Growth: Strong focus on professional development and training.
- Inclusive Culture: Embraces diversity with a Total Self culture where employees can authentically be themselves.
- Impactful Work: Contribute to life-changing therapies and innovative clinical research.
Job Description
Key Responsibilities
- Write, edit, and compile medical writing deliverables such as:
- Clinical study protocols & amendments
- Clinical study reports (CSRs)
- Patient narratives
- Investigator brochures (IBs)
- Review statistical analysis plans (SAPs) and ensure consistency with regulatory standards.
- Collaborate with biostatistics, data management, and regulatory teams to produce high-quality documents.
- Ensure compliance with ICH-E3, FDA guidelines, and company/client templates.
- Conduct clinical literature searches to support document development.
- Manage project timelines and budgets effectively.
Qualifications & Skills
- Bachelor’s degree in Science (Biology, Pharmacy, Medicine) or Arts (English, Communications, Social Sciences).
- Strong knowledge of AMA style guide and medical writing best practices.
- Familiarity with FDA & ICH regulations (preferred).
- Excellent proofreading, editing, and presentation skills.
- Proficiency in Microsoft Word, Excel, PowerPoint.
- Ability to interpret clinical data and present complex information clearly.
Work Model & Location
📍 Hybrid (Gurugram, India)
🕒 Minimal travel (<25%)
How to Apply?
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