About this role
Role Overview
- 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 of pharmacovigilance policies as needed
- Function as Pharmacovigilance subject matter expert for assigned product group(s)
Requirements
- Minimum requirement of a Veterinary Medicine (DVM, VMD)
- 5 or more years of experience in Veterinary Pharmaceutical Industry including veterinary pharmacovigilance in the US and/or EU
- Additional graduate degree or diploma in animal science and/or epidemiology or related experience is a plus
- Ability to review and analyze pharmacovigilance data to develop trending reports is essential
- Knowledge of the FDA/USDA and international regulations on Adverse Drug Event (ADE) reporting is a benefit
- Experience with database software and pharmacovigilance systems is desirable
Benefits
- healthcare and insurance benefits beginning on day one
- 401K plan with a match and profit-sharing contribution from Zoetis
- 4 weeks of vacation