Overview Pharmacovigilance Senior Specialist role at MSD . Based in Singapore, the regional hub for Asia Pacific (AP).
Our Clinical Research and Pharmacovigilance team pushes the boundaries of global healthcare through research and innovation. Through clinical trials and surveillance, we ensure the safety and efficacy of our existing and pipeline products to provide safe, effective, innovative medicine.
What You Will Do - Responsible for adverse event management including aggregate and individual case safety report (ICSR) health authority submissions and compliance monitoring.
- Manage day-to-day case processing for your assigned product portfolio, ensuring alignment with local laws and regulations.
- Collaborate with colleagues to adjust schedules and ensure continuous and complete adverse event reporting and drug safety oversight.
- Serve as the back-up Qualified Person for PV (QPPV) / Local Responsible PV person a...