THE POSITIONYou 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 orientedWHY THIS IS A GREAT PLACE TO WORKBoehringer 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. To learn more visit:https://www.Boehringer-ingelheim.Co.Uk/careers/uk-careers/why-great-place-work