Manager, Medical Information

Responsibilities Manage dissemination of medical information correspondence for multiple therapeutic areas to external (healthcare professionals) and internal customers within the pharmaceutical regulatory framework. Conduct and critically evaluate literature searches and scientific data. Prepare standard response documents; continuously update the standard response letter database. Ensure projects complete on schedule per established procedures and timelines. Create and review medical summaries of published literature for standard response letters. Support and guide responses to a vendor call center, including general training. Work within relevant and newly published FDA guidance for medical information. Lead and/or contribute to Medical Information planning for new product launches, line extensions, and key data releases. Provide logical recommendations and solutions for medical information activities. Provide Medical Information support at conference booths and learn booth processes. Collaborate cross-functionally with Medical Affairs/Regulatory/Pharmacovigilance as needed. Execute AMCP dossier requests with HEOR and field medical teams. Assist with ad-hoc Medical Information oversight and project coordination with minimal direction. Business travel (~10%) for scientific congresses and/or internal meetings. Qualifications Bachelor’s degree required; advanced degree (PharmD, PhD, etc.) preferred. Fellowship in Medical Information or at least 2 years related Medical Information experience in the pharmaceutical industry preferred. Excellent verbal, written, and interpersonal skills. High attention to detail. Strong task management skills (planning, prioritization, objective setting, meeting management) strongly preferred. Ability to support management and build effective stakeholder relationships. Critical thinking with ability to anticipate issues and impacts. Proficiency in Microsoft Excel, PowerPoint, and Word; strong working knowledge of databases. #J-18808-Ljbffr