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A leading pharmaceutical company in Berkshire is seeking a Medical Information Manager to provide comprehensive responses to medical inquiries and ensure compliance with industry standards. The role entails extensive collaboration and information management, critical for supporting product expertise and maintaining regulatory adherence in a hybrid working environment.
An excellent opportunity for an experienced Medical Information Manager to join a well-established Pharma company in Berkshire. The Medical Information Manager provides accurate, unbiased, balanced, and timely responses to unsolicited medical and clinical inquiries regarding the company's products from healthcare professionals, ensuring appropriate content and standards are maintained.
Within this position, you will have a wide range of responsibilities, including supplying medical information in response to internal and external customer inquiries, updating and creating scientific response documents related to the company's global and regional products, and providing specialist product knowledge to support the business. You will also support with copy approvals, job bag management, and related tasks.
This role involves internal engagement with colleagues in Medical Affairs, Regulatory, Commercial, Quality, Supply, Market Access, and Brand teams. You will support the Medical Information team with content development, repository management, intranet updates, and tracking.
The position offers a hybrid working policy, with 1 day per week in the office.
Key requirements include Medical Information response writing skills, handling medical information inquiries, knowledge of Medical Information procedures, EFPIA and ABPI codes, literature searching, and journal scanning. Experience with IRMS medical information database, medical compliance, and medical writing is highly desirable. The role demands attention to detail, project leadership, multitasking, and collaboration across multidisciplinary teams.
You will also provide product training to service providers, liaise with stakeholders to develop product expertise, contribute to cross-functional meetings, serve as an educational resource, attend external conferences, and perform copy reviews of promotional and non-promotional materials. Compliance with SOPs, regulations, and codes such as EFPIA, PIPA, Data Protection Act, and pharmacovigilance standards is essential.