Pharmacovigilence Trainee
- Daman & Diu
- Permanent
- Full-time
- Organize, manage and maintain a highly compliant pharmacovigilance (PV) System
- Should get involved in clinical trial activities
- Collection of information pertaining to the safety and efficacy of marketed product
- Revises product monograph, draft response to pharmacovigilance request from regulatory agencies, advises and inform health professional about product safety
- Prepare, reviewing and finalization of aggregate safety report for assigned product such as PSUR, DSURs, PV Plans, Risk Evaluation and RMPs
- Responsible for taking part in inhouse training session meeting Looking forward for good CVs.
- Logical thinking.
- Organizing.
- Good in communication.