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A well-established Pharma company is looking for a Medical Information Manager to oversee the accurate and timely responses to medical inquiries. This hybrid role allows for engagement across Medical Affairs and Regulatory teams, ensuring compliance and supporting product knowledge dissemination. Ideal candidates will have expertise in medical compliance, writing, and project management.
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Bolton, Greater Manchester, United Kingdom
Other
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Yes
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2
06.06.2025
21.07.2025
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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. You will supply medical information in response to internal and external customer inquiries. You will update and/or create scientific response documents pertaining to the company's global and regional products. Your role will also require you to provide specialist product knowledge to the business as a whole, thereby further contributing to the company's success. This position will also support the business with copy approvals, job bag management, and related tasks.
This is an all-encompassing Medical Information role, with a focus on internal engagement with colleagues in Medical Affairs, Regulatory, Commercial, Quality, Supply, Market Access, and Brand teams.
Support the Medical Information team with content development, repository updates, intranet pages, tracking, etc.
The role offers a great hybrid policy with 1 day per week in the office.
Requirements include Medical Information response writing skills, handling medical inquiries, knowledge of Medical Information, EFPIA and ABPI Codes and regulation, literature searching, journal scanning, and familiarity with IRMS medical information database. Strong knowledge of medical compliance, medical writing experience, project management skills, and the ability to collaborate across teams are essential.
The role involves training, stakeholder liaison, participation in conferences, copy review, and ensuring compliance with relevant SOPs, regulations, and codes.