THE POSITION 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.
Ensure all your application information is up to date and in order before applying for this opportunity.
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.
To learn more visit: https://www.boehringer-ingelheim.co.uk/careers/uk-careers/why-great-place-work