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Pharmacovigilance Trainee
2 weeks ago
Key responsibilities:
1. Report and document adverse drug reactions
2. Enter safety data into databases
3. Assist in preparing regulatory reports
4. Review medical literature for drug safety updates
5. Support safety analysis and risk management
- Minimal Customer interaction under guidance.
- Understand domain Process/sub-process, functions, and terminologies (such as SOP and QC checklists).
- For PV/Complaints Management, Individuals in this role enter data received from Source documents into the respective Clinical/Safety database. While performing this activity, the associate is responsible for meeting turnaround times and accuracy.
**Job Types**: Full-time, Permanent, Fresher
Pay: ₹10,000.00 - ₹12,000.00 per month
Schedule:
- Day shift
**Education**:
- Bachelor's (preferred)
**Language**:
- Any (preferred)
**Location**:
- Pune, Maharashtra (preferred)
Work Location: In person