Summary
This position will be responsible for receipt, distribution and tracking of adverse event/drug experience reports (serious and non-serious) and other safety related data for Incyte marketed products and clinical trials. The position will be responsible for the maintenance of all receipt channels and sources to ensure timely distribution of information for global Pharmacovigilance Operational teams. The position will also be responsible to liaise with relevant parties (external reporters, intradepartmental, external service provider/vendor or business partners) for related Pharmacovigilance information intake and distribution tasks as required.
Duties and Responsibilities
Requirements