Job Responsibilities:
- Conduct comprehensive literature reviews to gather and analyze scientific and clinical information
- Prepare and develop clinical study protocols in accordance with regulatory guidelines
- Create and maintain Investigator’s Brochures with accurate and up-to-date study data
- Write detailed Clinical Study Reports (CSRs) based on trial results
- Develop high-quality scientific manuscripts for publication in journals
- Ensure all documents meet regulatory, ethical, and quality standards
- Collaborate with cross-functional teams including clinical, regulatory, and research teams
Job Type: Full-time
Pay: ₹15,000.00 - ₹28,000.00 per month
Benefits:
- Health insurance
- Provident Fund
Experience:
- total work: 1 year (Preferred)
Work Location: In person
