Senior Pharmacovigilance Specialist, Regulatory Intelligence and Submissions - Based in Brazil

*MUST BE BASED IN BRAZIL AND FLUENT IN ENGLISH* The Senior Pharmacovigilance (PV) Specialist, Regulatory Intelligence (RI) and Submissions is responsible for adverse event submission and tracking of adverse event reports and periodic reports, maintenance of adverse event submission and exchange compliance, testing for health authority submission, process testing for submitting adverse event cases to new territories and/or for new product types, assigned safety reporting regulations research and…