PV Medical Manager

Zoetis

Regulatory Manager contributing to global pharmacovigilance activities in the veterinary pharmaceutical sector. Collaborating on ADE reports, safety evaluations, and regulatory agency submissions.

Posted 4/14/2026full-timeRemote • 🇺🇸 United StatesMid-LevelSenior💰 $114,000 - $185,000 per yearWebsite

About the role

Key responsibilities & impact

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
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
Prepare trending reports of assigned marketed products to the pharmacovigilance stakeholders and make recommendations regarding potential safety and efficacy profile adjustments
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
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 as necessary
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

Requirements

What you’ll need

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
Strong interpersonal skills, ability to work under pressure and in a highly matrix environment is essential
May lead/mentor others.

Benefits

Comp & perks

healthcare and insurance benefits beginning on day one
a 401K plan with a match and profit-sharing contribution from Zoetis
4 weeks of vacation

ATS Keywords

✓ Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools

pharmacovigilanceadverse drug experience reportingsignal detectiondata analysistrending reportsregulatory submissionrisk mitigationpharmacovigilance policieshealth hazard assessmentsveterinary pharmacovigilance

Soft Skills

interpersonal skillsability to work under pressurementoringcollaborationcommunicationproblem-solvingattention to detailadaptabilitycritical thinkingteamwork

Certifications

DVMVMDgraduate degree in animal sciencediploma in epidemiology