As a Pharmacovigilance (PV) Senior Specialist, you will be responsible for adverse event management including aggregate and individual case safety report (ICSR) health authority submissions and compliance monitoring. You will be responsible for day-to-day case management activities for your assigned product portfolio as applicable. You will collaborate with colleagues to ensure compliance with local laws and regulations, as well as adjusting schedules to support your colleagues to ensure there is no gap in adverse event reporting and drug safety oversight. WHAT YOU WILL DO Serves as the back-up Qualified Person for PV (QPPV) / Local Responsible PV person as required per local PV legislation. Serves as the point of contact for the local Health Authority for PV related questions from the Health Authorities (when assigned). Oversees all daily PV processes and activities within the countries covered by the country operation as required. Establishes and coordinates reconciliation activities...