Medical Information Senior Manager

Vertex PharmaceuticalsBoston, MA
Hybrid

About The Position

General Summary: The Medical Information Senior Manager drafts and maintains medical information content for use by the Medical Information Call Center (MIC) staff to respond to medical inquiries from healthcare professionals and patients. The Medical Information Senior Manager reviews MIC case records for accuracy of response and appropriate case processing in compliance with applicable policies, SOPs and country-specific regulations and/or guidance. Key Duties and Responsibilities: Develops and maintains in-depth therapeutic knowledge of disease, epidemiology, product and competitor product information to facilitate the creation of medical content. Drafts standard medical response letters and frequently asked questions (FAQs) for assigned product(s) and/or investigationals that are timely, non-misleading, accurate, and scientifically balanced for assigned Vertex marketed products and/or investigationals and relevant disease-related topics for use by MICs to respond to commonly received unsolicited medical inquiries. ' Provides guidance to Medical Information Managers on the appropriate methods for drafting standard medical responses (letters and FAQs). Works cross-functionally with other subject matter experts (SMEs) in Medical Affairs, Regulatory Affairs, Formulations and Pharmacovigilance to send response drafts (letters and FAQs) for review and approval to ensure drafts are accurate, compliant and appropriately address the topic of the inquiry. Creates standard language templates based upon SME review and approval. Utilizes therapeutic knowledge and clinical expertise to independently draft timely, non-misleading, accurate, and scientifically balanced custom responses to new and/or unusual unsolicited medical information inquiries concerning assigned product(s). Provides guidance to Medical Information Managers on the appropriate methods for drafting custom medical responses. Reviews medical information call center case records (medical inquiries, potential adverse events, and potential product complaints) to ensure quality and accuracy of response and appropriate case processing. Drafts metric and insight reports for use by medical information upper management and strategic business partners. Fact checks medical and marketing content, related to assigned product(s) and/or investigationals in the electronic review and approval system, for accuracy and appropriateness and relays all discrepancies to the appropriate subject matter expert or final approver. Monitors the medical literature for additional sources of product information and content for use in the creation of medical information materials

Requirements

  • Excellent oral and written communication and literature searching skills to explain difficult information
  • Experience drafting medical information content with a high degree of accuracy and accountability
  • Sound knowledge of the stages of drug development and the available corporate and public resources used to construct a medical information response
  • Ability to work collaboratively in a dynamic, team-based matrix environment and to function independently as appropriate
  • Strong working knowledge of the rules and regulations governing the provision of Medical Information in Pharma
  • Analytical skills and an ability to synthesize data sets and study summaries into meaningful oral or written communication materials
  • Bachelor’s degree in a health-related science
  • Typically requires 6 years experience, with 2 years experience working in either Medical Information or Medical Affairs in a biotech/pharma or equivalent combination of education and experience.

Responsibilities

  • Develops and maintains in-depth therapeutic knowledge of disease, epidemiology, product and competitor product information to facilitate the creation of medical content.
  • Drafts standard medical response letters and frequently asked questions (FAQs) for assigned product(s) and/or investigationals that are timely, non-misleading, accurate, and scientifically balanced for assigned Vertex marketed products and/or investigationals and relevant disease-related topics for use by MICs to respond to commonly received unsolicited medical inquiries.
  • Provides guidance to Medical Information Managers on the appropriate methods for drafting standard medical responses (letters and FAQs).
  • Works cross-functionally with other subject matter experts (SMEs) in Medical Affairs, Regulatory Affairs, Formulations and Pharmacovigilance to send response drafts (letters and FAQs) for review and approval to ensure drafts are accurate, compliant and appropriately address the topic of the inquiry.
  • Creates standard language templates based upon SME review and approval.
  • Utilizes therapeutic knowledge and clinical expertise to independently draft timely, non-misleading, accurate, and scientifically balanced custom responses to new and/or unusual unsolicited medical information inquiries concerning assigned product(s).
  • Provides guidance to Medical Information Managers on the appropriate methods for drafting custom medical responses.
  • Reviews medical information call center case records (medical inquiries, potential adverse events, and potential product complaints) to ensure quality and accuracy of response and appropriate case processing.
  • Drafts metric and insight reports for use by medical information upper management and strategic business partners.
  • Fact checks medical and marketing content, related to assigned product(s) and/or investigationals in the electronic review and approval system, for accuracy and appropriateness and relays all discrepancies to the appropriate subject matter expert or final approver.
  • Monitors the medical literature for additional sources of product information and content for use in the creation of medical information materials

Benefits

  • This role is eligible for an annual bonus and annual equity awards.
  • Some roles may also be eligible for overtime pay, in accordance with federal and state requirements.
  • From medical, dental and vision benefits to generous paid time off (including a week-long company shutdown in the Summer and the Winter), educational assistance programs including student loan repayment, a generous commuting subsidy, matching charitable donations, 401(k) and so much more.
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