THThepharmadaily
Medical Writer
Mohali ₹8-13 LPA Posted 13 Aug 2025
FULL TIME
Medical Writing
Ct
Regulatory Requirements
icf
Job Description
- Writing clinical trial (CT) protocols.
- Designing case report forms (CRF).
- Preparing informed consent forms (ICF).
- Compiling and preparing clinical trial reports.
- Ensuring all documents comply with regulatory requirements and industry standards.
- Collaborating with clinical teams to ensure accuracy and clarity in documentation.
- Conducting literature reviews to support clinical documents.
- Assisting in the development of study-related materials.
- Reviewing and editing documents to ensure consistency and quality.
- Qualifications2-3 years of experience in medical writing.
- CompensationAnnual salary ranging from 4-6 Lacs.