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The Director of Pharmacometrics leads quantitative analyses in drug development across therapeutic areas and ensures adherence to timelines and budgets for pharmacology studies.

The AGC Development Counsel partners with Gilead's Development organization, providing legal counsel on regulatory matters, overseeing compliance, and managing legal risks associated with drug development.

Serve as Lead AI Counsel, providing strategic legal advice on AI and technology regulations, guiding IT and business teams in a highly regulated industry, fostering inclusion and talent development, and ensuring compliance with evolving laws.

As a Senior Associate Scientist, QC Analytical at Gilead, you'll support Clinical Biologics QC through testing coordination, data management, method validation, and compliance with regulations.

Manage and govern Gilead's global publications database (iEnvision): maintain system compliance, run audits and global/regional publication metrics, develop and deliver training, coordinate vendor enhancements, maintain SharePoint resources, support budgeting and ensure adherence to publication policies and good publication practices.

Lead human factors engineering strategies for medical device development, conduct usability studies, ensure regulatory compliance, and improve internal processes.

Lead strategy and execution for clinical systems and analytics (Veeva, Medidata, Salesforce, cloud platforms). Oversee large technical programs, scalable data architectures, compliance with GxP, cross-functional stakeholder alignment, budgeting, and people leadership to deliver analytics-ready clinical data and drive operational improvements.

The Associate Director, Generative AI will lead AI product development within Gilead's commercial functions, focusing on governance and collaboration across teams while handling revenue forecasting and brand analytics in the pharmaceutical domain.

The Sr. Quality Assurance Specialist provides quality oversight for GxP quality records related to facilities and engineering systems, ensuring compliance with cGMP standards and managing deviation investigations and CAPAs while collaborating across engineering and quality teams.

The role involves leading market access strategies, payer engagement, and cross-functional collaboration to enhance therapy access in alignment with Gilead's goals. Responsibilities include strategic planning, communication strategy development, and managing payer insights.