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
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