Clinical protocol writer

Job Description: Clinical Protocol Writer

Location: Navi Mumbai
Department: Clinical Research / Medical Writing
Type: Full-time
Industry: USFDA-compliant Analytical & Bioanalytical Laboratory

Position Overview

The Clinical Protocol Writer is responsible for developing high-quality clinical study documents in accordance with USFDA, ICH-GCP, and global regulatory standards. The role involves collaborating with cross-functional teams—including clinical operations, bioanalytical scientists, statisticians, and quality assurance—to prepare clinical protocols, amendments, investigator brochures, informed consent forms, and related regulatory documents.

Job Type: Full-time

Pay: ₹250,000.00 - ₹900,000.00 per year

Benefits:

• Provident Fund

Work Location: In person