01Responsibilities
- Collect and process adverse event reports from clinical trials and post-marketing sources
- Perform case triage, data entry, and quality checks in safety databases
- Assist in preparation of regulatory reports (e.g., CIOMS, MedWatch)
- Conduct literature screening for safety data
- Ensure compliance with global pharmacovigilance regulations and SOPs
Job Types: Full time, Fresher
Compensation: 286,000.00 - 970,000.00 per year
Benefits:
- Health insurance
Schedule:
- Day shift
Work Location: In person .
