PV Medical Manager – Deputy QPPV

🔥 7 minutes ago

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Zoetis

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1952

🧬 Biotechnology

💊 Pharmaceuticals

🔬 Science

Biotechnology • Pharmaceuticals • Science

Zoetis is the world's leading animal health company, committed to nurturing the world and humankind by advancing care for animals. With over 70 years of innovation, Zoetis develops a broad portfolio and pipeline of medicines, vaccines, diagnostics, and technologies that span a continuum of care to predict, prevent, detect, and treat animal illnesses. Operating in more than 100 countries, the company supports livestock farmers, veterinarians, and pet owners around the globe. Zoetis is driven by science and their shared passion for the human-animal bond, aiming to create a more sustainable and healthier world for all.

📋 Description

• Contributor to a Global Team with collective responsibility for regulatory activities associated with global pharmacovigilance • 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 from a data capture, trend analysis and regulatory submission perspective • Function as Pharmacovigilance subject matter expert for assigned product group(s) • Provide pharmacovigilance input for advertising and promotional material upon request • Risk Mitigation in support of Global Manufacturing and Quality and Regulatory label defense activities • Complete PV Data requests and Health Hazard Assessments for assigned products upon request • Act as Deputy EU/UK QPPV

🎯 Requirements

• Minimum requirement of a Veterinary Medicine (DVM, VMD) • 5 or more years of experience in Veterinary Pharmaceutical Industry including veterinary pharmacovigilance in the European Union • Ability to review and analyze pharmacovigilance data to develop trending reports • Knowledge of the FDA/USDA and international regulations on Adverse Drug Event (ADE) reporting is a benefit • Strong interpersonal skills • Experience with database software and pharmacovigilance systems is desirable

🏖️ Benefits

• Competitive healthcare and retirement savings benefits • an array of benefits, policies and programs to support employee well-being in every sense, from health and financial wellness to family and lifestyle resources