Medical Writer Job at Cliantha Research in Ahmedabad | Jobslly

Role & Responsibilities
• Prepare protocols, CSRs, and regulatory documents
• Ensure compliance with ICH-GCP guidelines
• Coordinate reviews and submissions

Qualification
• B.Pharm / M.Pharm / Pharm.D / M.Sc Life Sciences

Experience
• 1–2 years in medical writing

Skills
• Scientific writing, regulatory knowledge, documentation

About the Company
Cliantha Research is a reputed CRO delivering regulatory and medical writing services.