Write study protocols, synopses, and Clinical Study Reports (CSRs) across Pharma Regulatory,
Observational, and Medical Device studies
- Draft quotations and scope-of-work documents to support Business Development proposals
- Prepare monographs and regulatory dossier content where required for client submissions
- Support manuscript writing and journal submission for sponsor publications
- Ensure all documents meet applicable regulatory (CDSCO, ICH) and journal formatting standards
- Coordinate document review cycles with Clinical Operations, Data Management, and Biostatistics for accuracy
- Maintain a document template library to standardise turnaround across study types
- Support literature review and background sections for protocols and manuscripts
Pay: ₹40,000.00 - ₹50,000.00 per month
Work Location: In person
