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Medical Information Manager, Portsmouth, Hampshire
Client:
Location:
Portsmouth, Hampshire, United Kingdom
Job Category:
Other
-
EU work permit required:
Yes
Job Views:
2
Posted:
06.06.2025
Expiry Date:
21.07.2025
Job Description:
An excellent opportunity for an experienced Medical Information Manager to join a well-established Pharma company in Portsmouth. 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.
Responsibilities include 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. The role also involves supporting the business with copy approvals, job bag management, and related tasks.
This is a comprehensive Medical Information role with a focus on internal engagement with colleagues across Medical Affairs, Regulatory, Commercial, Quality, Supply, Market Access, and Brand teams.
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, including 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, including EFPIA and ABPI Codes.
* Expertise in literature searching and journal scanning.
* Understanding of IRMS medical information database (desirable).
* Excellent knowledge of medical compliance.
* Experience in medical writing (preferred).
* Detail-oriented with project management and multitasking abilities.
* Providing product training and liaising with stakeholders to develop product expertise.
* Collaborating with Medical Affairs and participating in cross-functional meetings.
* Representing the company at external medical conferences.
* Performing copy review of promotional and non-promotional materials.
* Ensuring compliance with SOPs, regulations, and codes, including EFPIA, PIPA, Data Protection Act, and Pharmacovigilance rules.
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