Jobs at Gilead Sciences

The Scientist will drive drug development for inflammatory diseases by designing experiments, analyzing data, and collaborating across team disciplines.

Lead antibody discovery initiatives in Protein Therapeutics using in silico methods, collaborating with teams on drug candidate selection and optimization. Manage a team and drive innovation in antibody discovery processes.

The Director, R&D Quality is responsible for strategic quality leadership, regulatory oversight for diagnostic programs, ensuring compliance with medical device regulations, and supporting R&D functions across various therapeutic areas.

The Sr Director leads the global procurement strategy, overseeing sourcing excellence, strategy execution, capability building, and ensuring alignment with corporate objectives. They manage teams, implement frameworks, and drive procurement transformation initiatives.

The Director will implement global HEOR strategies for HIV, support commercialization, conduct studies, and guide cross-functional collaborations.

The Director of Global Compliance Systems & Analytics will define business needs, drive user adoption, and ensure compliance systems provide sustained value and insights, enhancing overall compliance effectiveness.

The Senior Director leads advocacy and communication strategies to enhance access to Gilead’s innovations in low-income countries, fostering partnerships and managing internal and external communications while navigating issues and reputation management.

The Associate Director will manage market research and analytics for Gilead's Lung Cancer portfolio, impacting commercial strategy and decision-making. Responsibilities include forecasting, market analysis, and partnership with stakeholders to ensure informed insights and successful launch strategies.

The Associate Director, Biostatistics leads statistical strategy for clinical trials, collaborates with multiple teams, and ensures statistical integrity in study designs and documentation.

The Director of Biostatistics will lead statistical leadership for Virology drug development, collaborating across departments for trial design, compliance, and strategy. Responsibilities include overseeing operational statistics, supporting regulatory interactions, and managing personnel development.

The Executive Director will oversee data science and data management strategies, leading capabilities across commercial insights and analytics while collaborating across multiple organizational functions.

The Director of Clinical Development leads clinical trials in HIV, provides scientific guidance, manages regulatory documentation, and ensures adherence to clinical standards.

Lead global procurement strategies and partnerships, manage teams, and drive value creation while fostering collaboration and diversity across Gilead's Procurement operations.

Lead Quality Engineer for medical device combination product development, focusing on design controls, risk management, and lifecycle quality oversight. Ensure compliance with regulatory standards and support cross-functional collaboration for product development.

The Director of Nonclinical Safety will oversee nonclinical safety programs, contribute to regulatory documents, manage multiple projects, and lead cross-functional teams in drug development.

The Senior Director, Project Management Group Lead leads CMC project management professionals at Gilead, overseeing drug development and commercialization, while managing risks and supporting talent development.

The Director, Quality Compliance and Audits leads Gilead's global audit program ensuring compliance with regulatory requirements. They manage a team, develop audit plans, monitor compliance risks, and collaborate with stakeholders to improve quality oversight.

The Sr Director is responsible for leading proactive quality strategies within a pharmaceutical context, ensuring compliance, improving processes, and embedding human-centric practices.

Lead the design of Data and AI solutions, partner with stakeholders, ensure scalable architectures, and adhere to regulatory standards within Gilead's PDM and Tech Ops.

The role involves owning the product vision for AI-enabled capabilities in clinical development. Responsibilities include stakeholder engagement, defining product requirements, prioritizing backlogs, and ensuring compliance with regulations while driving user adoption and continuous improvement.