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
Perks:
Health insurance
Schedule:
Day shift
Work Location: In person .
