Medical Information Specialist

Description

• Mentor and train the Medical Information team, assign responsibilities, and ensure achievement of individual business objectives.
• Support in implementing the global strategy of MI and support localizing some strategic imperatives with the aim to leverage Medical Information for a competitive business advantage.
• Partner with Global Medical Information and other R/OPUs to identify new channels to disseminate medical information for increased impact and efficiency.
• Manage the external, stakeholder-facing Medical Information website and ensure availability of standard response documents are accessible via the website, if warranted.
• Participate in the Medical Legal Review (MLR) of material regarding BI's products and disease states for medical and scientific accuracy.
• Report Adverse Events (AEs) and Product Complaints that arise from Medical Information interactions within required timelines.

Qualifications

• Handling and implementation of tasks related to the Medical Information team, to ensure the provision of accurate, factual, balanced, high quality Medical Information for BI products to healthcare professionals, patients, as well as internal colleagues
• This would also entail mentorship and training to the other members of the Medical Information team including the Intern. Ensure, sufficient back-up to perform all Medical Information functions during absences
• Develop local strategies with colleagues to identify opportunities to leverage Medical Information for a competitive business advantage
• Partner with Global Medical Information colleagues to identify new channels to disseminate medical information for increased impact and efficiency
• Manage the external, stakeholder-facing Medical Information website and ensure availability of standard response documents are accessible via the website, if warrantedDevelop or adapt global standard response documents in correspondence with Canadian medical and regulatory context and ensure their availability on the external Medical Information website, if warranted
• Participate in the Medical Legal Review (MLR) process to review dockets for compliance and medical accuracy
• Report adverse events and Product Complaints that arise from Medical Information interactions within required timelines