Full Time
Medical Writer
Cliantha Research
Ahmedabad
₹4 - ₹18 LPA
Posted 05/01/2026
About the Role
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.
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