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)

TASK & RESPONSIBILITES

• 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.

• Develop an appropriate level of knowledge of technical aspects of all portfolio products and a general understanding of disease conditions appropriate to their use to ensure that cases are entered accurately.

REQUIREMENTS

• Ability to understand scientific/clinical data

• Strong planning and prioritsation skills

• Process orientated

• Excellent communication and interpersonal skills and strong team ethos.

• Analytical and detail oriented

WHY THIS IS A GREAT PLACE TO WORK

Boehringer Ingelheim has been recognised as a Top Employer in the UK. Being certified as a Top Employer confirms our dedication to a better world of work, delivered through excellent HR policies and people practices.