Responsibilities Respond to unsolicited medical requests about Gilead products from HCPs, the public, and internal colleagues using approved resources in a timely manner. Use scientific and MI expertise to support strategic initiatives and enable timely, informed decisions and improved patient outcomes. Perform 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 per SOP. Contribute to GMI strategy and represent GMI cross-functionally; may lead global projects/initiatives/product launches. Routine Responsibilities Maintain deep knowledge of products/disease/competitor landscape for assigned therapeutic area. Handle medical/scientific information requests; research complex cases with cross-functional teams. Create/update/review/approve MI response documents; maintain approved document repository. Collaborate with internal partners (e.g., medical affairs, development, regulatory, patient safety, commercial) to manage response content. Analyze MI databases for trends/insights; prepare customer interaction reports; support congress booths; serve as SME. Qualifications Basic: 10+ years with BS/BA OR 8+ years with MS/MA or MBA. Preferred Qualifications / Skills PharmD/MD/PhD or equivalent; MI or comparable healthcare/clinical experience; pharmaceutical/MI vendor experience. Experience in medical/promotional reviews; strong written/verbal/interpersonal skills; ability to analyze clinical/scientific data; regulatory/legal knowledge for MI; attention to detail, project management, problem-solving. Benefits Annual bonus/LTIs/paid time off; medical/dental/vision/life insurance; salary range: Bay Area $195,670–$253,220; other US locations $177,905–$230,230. #J-18808-Ljbffr