Assoc Director, Medical Information

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 may include:
- 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).

Application instructions:
- Apply via the Internal Career Opportunities portal in Workday (for current employees/contractors).