Medical Manager

Zoetis

Contributing to global pharmacovigilance activities as part of Zoetis. Collaborating on regulatory activities and providing input on safety and efficacy of products post-marketing.

Posted 4/15/2026full-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
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

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

Benefits

Comp & perks

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

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

pharmacovigilancedata analysisreportingregulatory submissionsignal managementtrending reportspolicy designadverse drug event (ADE) reportingveterinary pharmacovigilanceanimal science

Soft Skills

collaborationcommunicationnegotiationsubject matter expertise

Certifications

DVMVMD