About this role
This position will be located in Spain, and it is required to live in Spain and have work permit.
Job Description
Contributor to a Global Team with collective responsibility for regulatory activities associated with global pharmacovigilance including electronic pharmacovigilance system, adverse drug experience (ADE) reports, trending reports, ADE submissions to CVM, pharmacovigilance SOPs, and Signal Management responsibilities.
Duties and Responsibilities include but not limited to:
1. Good understanding of the ADE reporting regulations (US and EU) and of product trending standards.
2. Collaborate with signal management team regarding validation activities for assigned products (including signal detection) to comply with FDA/USDA/EU expectations and to better understand the safety and efficacy profiles of Zoetis products post-marketing.
3. Prepare trending reports of assigned marketed products to the pharmacovigilance stakeholders and make recommendations regarding potential safety and efficacy profile adjustments.
4. Provide input for negotiations with regulatory agencies regarding submission of ADE reports as well as for responses to these agencies about product safety and efficacy issues.
5. Assist in the design pharmacovigilance policies as needed.
8. Assist in the maintenance of a pharmacovigilance electronic system from a data capture, trend analysis and regulatory submission perspective as necessary.
9. Function as Pharmacovigilance subject matter expert for assigned product group(s).
10. Provide pharmacovigilance input for advertising and promotional material upon request.
11. Risk Mitigation in support of Global Manufacturing and Quality and Regulatory label defense activities.
12. Complete PV Data requests and Health Hazard Assessments for assigned products upon request.
13. Act as Deputy EU/UK QPPV
Minimum requirement of a Veterinary Medicine (DVM, VMD) and 5 or more years of experience in Veterinary Pharmaceutical Industry including veterinary pharmacovigilance in the European Union. 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. Strong interpersonal skills, ability to work under pressure and in a highly matrix environment is essential.
Experience with database software and pharmacovigilance systems is desirable. May lead/mentor others.
Full timeRegularColleagueAny unsolicited resumes sent to Zoetis from a third party, such as an Agency recruiter, including unsolicited resumes sent to a Zoetis mailing address, fax machine or email address, directly to Zoetis employees, or to Zoetis resume database will be considered Zoetis property. Zoetis will NOT pay a fee for any placement resulting from the receipt of an unsolicited resume.
Zoetis will consider any candidate for whom an Agency has submitted an unsolicited resume to have been referred by the Agency free of any charges or fees. This includes any Agency that is an approved/engaged vendor but does not have the appropriate approvals to be engaged on a search.
Other facts
About Zoetis
The world’s leading animal health company. We’ve been innovating ways to predict, prevent, detect, and treat animal illness for over 70 years, and we continue to stand by those raising and caring for animals worldwide – from veterinarians and pet owners to livestock farmers. Our leading portfolio and pipeline makes a difference in over 100 countries.
Community Guidelines:
This page is intended to share how Zoetis is advancing care for animals. We aspire to create a supportive community, but there are guidelines to which posts and comments on this page must adhere.
If your post references a side effect related to any Zoetis product, we may contact you for more information. To monitor the safety of Zoetis products, we advise you to call our Veterinary Medical Information and Product Support Team at 1-888-963-8471; Support Team is available Mon-Fri 9am to 6:30pm ET.
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What you'll do
- The role involves contributing to global pharmacovigilance activities, including ADE reporting and signal management. The candidate will also prepare trending reports and provide input for negotiations with regulatory agencies.
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