- Prepare and review study-related documents i.e. Protocol, ICD, CRF, and all other relevant documents in accordance with regulatory compliance.
- Records and Data compilations/Writings to support clinical study regulatory requirements needed for drug development and registration process.
- Performing Project Coordination, Project Planning, and its execution and management
Location: Gandhinagar, Ahmedabad
Qualification: B.Pharma, M.Pharma
Experience: 2-5 Years