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, update and create scientific response documents related to the company's global and regional products, and provide specialist product knowledge to support the business's success. The role also involves supporting the business with copy approvals, job bag management, and related tasks.
This is a comprehensive Medical Information role, focusing on 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 role offers a hybrid working policy, with 1 day per week in the office.
Key skills and requirements include:
* Medical Information response writing, including style, order, clinical paper summaries, readability, and compliance.
* Handling medical information inquiries and maintaining systems for recording these inquiries, developing standard responses for FAQs.
* Knowledge of Medical Information procedures.
* Understanding of EFPIA and ABPI Codes and regulations.
* Expertise in literature searching and journal scanning to identify key papers.
* Strong understanding of IRMS medical information database (desirable).
* Excellent knowledge of medical compliance.
* Medical writing experience (strongly preferred).
* Attention to detail, project leadership, multitasking, and collaboration with multidisciplinary teams.
* Providing product training to service providers and collaborating as needed.
* Liaising with stakeholders to develop and maintain product expertise.
* Participating in cross-functional meetings and group discussions.
* Serving as an educational resource internally and externally.
* Attending external medical conferences and staffing Medical Information booths as needed.
* Performing copy reviews of promotional and non-promotional materials.
* Ensuring compliance with SOPs, regulations, and codes such as EFPIA, PIPA, Data Protection Act, and Pharmacovigilance rules.
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