Key Responsibilities:
- Supporting clinical trial planning and execution
- Preparation of study documents such as protocols, CRFs, and SOPs
- Monitoring and ensuring data integrity during clinical studies
- Pharmacovigilance activities including AE/SAE reporting
- Coordination with investigators, ethics committees, and regulatory bodies
Experience : 1-2 Years of Relevant Experience.
Required Qualification : M.Pharma
Work Location: In person
