Medical Writer Jobs: Build Your Medical Writing Career with Syneos Health
Join Syneos Health, a global leader in biopharmaceutical solutions, as a Medical Writer II (CSR Narratives). This full-time remote position is ideal for experienced professionals skilled in preparing and reviewing clinical study documents, narratives, and reports in compliance with regulatory standards such as ICH and FDA guidelines. At Syneos Health, you’ll collaborate with a diverse team of experts across 110 countries to accelerate therapeutic development and improve patient outcomes. Apply now for Syneos Career and enhance your medical writing skills.
Job Details:
- Job Title: Medical Writer II (CSR Narratives)
- Location: Remote – Pune, Maharashtra, India
- Employment Type: Full-time
About Syneos Health
Syneos Health® is a leading fully integrated biopharmaceutical solutions organization dedicated to accelerating customer success. The company combines clinical, medical affairs, and commercial insights to address real-world healthcare challenges. With a presence in over 110 countries and 29,000 employees, Syneos Health is driven by a mission to simplify and optimize clinical development for patients worldwide. At Syneos Health, work here matters everywhere. The organization nurtures a Total Self culture, promoting authenticity, inclusion, and growth. Employees benefit from strong career development programs, therapeutic area training, peer recognition, and supportive management.
Education:
Postgraduate (Masters/M.Pharm) or Graduate degree in a Life Science discipline preferred.
Key Responsibilities:
- Mentor junior medical writers and provide guidance on assigned projects.
- Compile, write, and edit clinical documents including Clinical study protocols and amendments, Clinical study reports, Patient narratives, and Annual reports and investigator brochures.
- Review statistical analysis plans and data listings for content and consistency.
- Collaborate with teams in data management, biostatistics, and regulatory affairs.
- Serve as a peer reviewer to ensure clarity, consistency, and adherence to templates.
- Ensure compliance with ICH-E3 guidelines, SOPs, and client standards.
- Conduct online clinical literature searches when needed.
- Maintain professional development and stay updated on regulatory guidance.
- Work within assigned project budgets and timelines.
- Perform other assigned duties with minimal supervision.
- Occasional travel (less than 25%) may be required.
Qualifications & Skills:
- Minimum 1 year of experience working in CSR narratives with a Master’s degree, or 2 years with a Bachelor’s degree.
- Strong knowledge of English grammar, FDA, and ICH regulations, with familiarity in AMA style guide.
- Excellent proofreading, presentation, and leadership skills.
- Strong proficiency in Microsoft Word, Excel, PowerPoint, and Internet research.
- Ability to interpret and present clinical data clearly.
