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/or create scientific response documents pertaining to the company's global and regional products, and provide specialist product knowledge to contribute to the company's success. The role also involves supporting 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.
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 skills; style, order, clinical paper summaries, readability, and compliance.
* Handling medical information inquiries and maintaining systems for recording these inquiries.
* Developing and maintaining standard responses to frequently asked questions.
* Knowledge of Medical Information procedures and regulations.
* Understanding of EFPIA and ABPI Codes and regulations.
* Expertise in literature searching and journal scanning for key papers.
* Strong understanding of IRMS medical information database (desirable).
* Excellent knowledge of medical compliance.
* Experience in medical writing (strongly preferred).
* Attention to detail, project leadership, multitasking, and teamwork skills.
* Providing product training to service providers and collaborating as needed.
* Liaising with stakeholders to develop and maintain product expertise.
* Collaborating with Medical Affairs and participating in cross-functional meetings.
* 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 of practice, including EFPIA, PIPA, Data Protection Act, Copyright, and Pharmacovigilance rules.
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