You will work within the Regulatory Affairs/Pharmacovigilance (PV) team to ensure all PV cases from our Animal Health business are collected and reported correctly.

12 month contract

This is a part time role for a 3 day a week position (2 day remote, 1 day on-site per week)

Ensure accurate case entry of suspected adverse events into the PV database in compliance with regulatory requirements and company SOPs.• Work closely with veterinary services team and other customer facing functions to ensure that suspected adverse reaction cases and related complaints are investigated, recorded and reported accurately.• Manage own caseload to ensure all cases are entered accurately, within timelines in compliance with regulatory requirements and company SOPs.• Develop understanding of pharmacovigilance processes, databases and regulatory requirements related to the role, particularly the strict recording and reporting timelines.• Ability to understand scientific/clinical data• Strong planning and prioritsation skills• Animal Health/Veterinary background essential

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