Responsibilities Respond to unsolicited medical requests about Gilead products from HCPs, members of the public, and internal colleagues using approved scientific response documents and up-to-date literature. Use scientific and MI expertise to drive strategic initiatives and empower partners, HCPs, and patients to support timely, informed decisions and improved patient outcomes. Perform appropriate medical review for promotional and/or medical materials. Prepare global scientific resources with local affiliate teams. Identify, report, and record adverse events and product complaints in accordance with SOP. Contribute to development of GMI strategy and represent GMI cross-functionally. May lead department-wide/global projects, initiatives, and product launches. Routine responsibilities Maintain deep knowledge of product, disease state, and competitor landscape for assigned therapeutic area. Respond to unsolicited medical/scientific information requests via the request handling system. Research and collaborate with cross-functional colleagues to address complex requests. Create, update, and participate in review/quality check/approval of MI response documents. Collaborate with affiliate MI and internal partners (e.g., medical affairs, development, regulatory, global patient safety/operations, commercial) to manage global response topics/content. Prepare/approve data on file to support response documents and complex requests. Maintain a document repository with routine review for new data (regulatory updates, conferences, literature surveillance, newly published materials). Analyze MI databases for trends, customer insights, and data gaps; prepare customer interaction reports. Support MI booths at scientific congresses. Serve as liaison for department-specific training for new staff/colleagues/vendors (as required). Support TA activities including product launches, labeling updates, and patient engagement. Execute and drive global MI initiatives to improve patient care. Serve as SME for one or more products or therapeutic areas. Build and cultivate relationships with appropriate functions. Basic qualifications 10+ years with BS/BA OR 8+ years with MS/MA or MBA. Preferred qualifications PharmD, MD, PhD, or equivalent. MI experience preferred (or comparable healthcare/clinical experience required). Experience in pharmaceutical industry or MI vendor. Experience conducting medical/promotional reviews. Excellent written, verbal, and interpersonal communication; ability to work in multidisciplinary teams across geographies. Ability to create and clearly communicate scientific data to different audiences. Knowledge of applicable regulatory and legal requirements for MI. Ability to analyze/evaluate clinical, biomedical, and scientific data. Strong attention to detail, project management, and problem-solving skills. Previous experience with problem-solving and project management. Benefits Company-sponsored medical, dental, vision, and life insurance plans (and may include discretionary annual bonus, discretionary stock-based long-term incentives, paid time off, and a benefits package). #J-18808-Ljbffr