Global Pharmacovigilance Medical Manager
Job Description: • Good understanding of the ADE reporting regulations (US and EU) • Collaborate with signal management team regarding validation activities for assigned products • Prepare trending reports of assigned marketed products to the pharmacovigilance stakeholders • Provide input for negotiations with regulatory agencies regarding submission of ADE reports • Assist in the design pharmacovigilance policies as needed • Assist in the maintenance of a pharmacovigilance electronic system Requirements: • DVM (Doctor of Veterinary Medicine) or equivalent veterinary degree • advanced degree (e.g., MSc, PhD) in pharmacology, toxicology, or related field • 3+ years of experience in the Pharmaceutical Industry • Experience with FDA/USDA and international regulations on Adverse Drug Event (ADE) reporting • Experience in reviewing and analyzing pharmacovigilance data to develop trending reports Benefits: • healthcare • dental coverage • retirement savings benefits • paid holidays • vacation • disability insurance