- Assist in entering safety data into pharmacovigilance databases (e.g., Argus, ARISg).
- Perform initial coding of medical terms using MedDRA and drugs using WHO-DD.
- Support the preparation of case narratives and regulatory reports.
- Ensure all activities comply with applicable regulatory guidelines (GVP, ICH, FDA).
- Participate in internal training programs to build knowledge in drug safety and pharmacovigilance practices.
- Collaborate with senior team members on various projects and documentation tasks.
Job Types: Full-time, Permanent, Fresher
Pay: ₹358,180.92 - ₹670,989.55 per year
Benefits:
- Health insurance
- Paid sick time
- Provident Fund
Work Location: In person