Responsibilities
- Manage the collection, data entry, and thorough processing of adverse event reports to ensure accuracy and timely handling.
- Verify MedDRA coding accuracy and develop detailed clinical narratives that clearly present case details.
- Submit Individual Case Safety Reports (ICSRs) to regulatory agencies within required legal timeframes.
- Conduct detailed quality reviews and assist in audit readiness to uphold high compliance standards.
- Provide guidance and mentorship to junior staff by sharing knowledge of pharmacovigilance procedures and best practices.
Work Arrangement
Hybrid
Other
- Shift: 8PM - 5AM (Weekends off)
- Start Date: ASAP
- Work Arrangement: Hybrid (Onsite during probationary period) | Cebu
