Job Description

We’re looking for an experienced Senior Medical Writer to join our Clinical and Regulatory Medical Writing team. The ideal candidate will have a strong scientific background, excellent writing skills, and proven experience in preparing high-quality clinical and regulatory documents that support drug development and regulatory submission.

Key Responsibilities:
Author and review clinical and regulatory documents (protocols, IBs, CSRs, CTDs, etc.)
Analyze and interpret clinical data to ensure scientific accuracy
Ensure compliance with ICH-GCP and global regulatory standards
Collaborate with cross-functional teams (clinical, regulatory, biostats, PV)
Mentor and review work of junior medical writers

Requirements:
Master’s or Ph.D. in Life Sciences, Pharmacy, or Medicine (PhD/MPharm preferred)
4–6 years of experience in medical writing within pharma/CRO/clinical research
Strong understanding of regulatory submissions (IND, NDA, MAA)
Excellent written and verbal communication skills
Proficiency in MS Office and document management tools (e.g., Veeva Vault, SharePoint)

Location: Ahmedabad
Department: Clinical and Regulatory Medical Writing

If you have a passion for scientific communication and a keen eye for detail, we’d love to hear from you!
📩 Apply now or share your resume at [shalini.maurya@nuvo.ai].