Jobs at Gilead Sciences

The Director, Epidemiology will lead the real-world evidence strategy for Inflammation products, ensuring timely execution and regulatory compliance for observational studies while managing cross-functional teams.

Promote Gilead therapies to healthcare professionals within an assigned territory, achieve sales and coverage targets, prepare territory business plans and budgets, collaborate cross-functionally (MSLs, marketing), represent the company at professional events, monitor sales progress, and ensure regulatory and commercial compliance.

Manage a portfolio of partnered R&D programs, lead cross-functional and collaborator meetings, track integrated timelines, identify risks and readiness for governance, support licensing/internalization and IP activities, and produce documentation and portfolio tracking materials to drive program success.

Territory-based pharmaceutical specialist responsible for achieving sales and coverage targets, managing budgets and events, collaborating cross-functionally, monitoring market dynamics, supporting training, and ensuring compliance with industry and company promotional regulations.

Support site process safety for API manufacturing: conduct process safety assessments, use thermal and calorimetry techniques (DSC, ARC, RC1), develop safe scale-up strategies, ensure cGMP/SOP compliance, and help build site process safety programs and training.

Serve as Global Process Owner for Gilead's Global Quality Agreement Program: develop and maintain templates and governance, ensure global regulatory compliance, lead negotiations and lifecycle management of Quality Agreements, support inspections and audits, drive continuous improvement, and train stakeholders across internal and external partners.

Lead Gilead's federal government affairs strategy and advocacy; advise senior leadership; build bipartisan relationships with Congress, the Administration, and agencies; translate policy into business guidance; coordinate cross-functional advocacy; lead the federal GA team, external consultants, and PAC; ensure lobbying, ethics, and compliance.

The Senior Director of Public Affairs, External Affairs will develop and execute communication strategies supporting legislative, regulatory, and public policy objectives while enhancing Gilead's reputation and stakeholder engagement.

Territory-based pharmaceutical sales role promoting Gilead HBV/HDV products to healthcare professionals in Minneapolis. Develop territory business plans, build relationships, deliver clinical education, achieve sales targets, report adverse events, and collaborate with internal teams while adhering to compliance and regulatory guidelines.

As a Senior Scientist, you will develop machine learning methods for biologics design, optimize large-molecule therapeutics, and work collaboratively with experimental teams to enhance drug development processes.

The Clinical Trials Manager is responsible for managing European/global activities in clinical trials, overseeing CROs, coordinating study documents, and ensuring regulatory compliance.

The Senior Regulatory Affairs Manager will represent regulatory affairs, define regulatory strategy, manage regulatory submissions, lead cross-functional teams, and ensure compliance with regulations.

The Senior Quality Assurance Specialist manages batch record reviews, assesses risks, ensures compliance with GMPs, and leads internal audits while supporting quality issue resolution and continuous improvement initiatives.

The Director of Biostatistics will lead statistical analysis for oncology trials, collaborate across teams, and ensure compliance in drug development.

The Postdoctoral Scientist will investigate HIV latency and reservoir dynamics using advanced molecular and cellular assays, focusing on proviral expression and inducing therapeutic strategies for HIV remission.

Develop scalable mammalian cell culture processes for biologics. Collaborate on optimizing cell culture media and lead experiments while maintaining lab practices.

The QA Specialist III will support SAP QM solutions, manage incidents, drive quality process optimization, and ensure compliance with regulatory requirements.

Develop chemical processes for manufacturing drug substances, execute laboratory experiments, manage project teams, and ensure compliance with quality standards.

The Senior Product Manager will lead the strategy and delivery of Workday Talent & Performance capabilities, focusing on product ownership and enhancing HR technology solutions for talent growth.

Lead non-promotional unbranded strategies in Virology focused on community engagement, disease awareness, Screening and Linkage to Care (SLTC), and partnerships with NGOs, providers and public health stakeholders. Translate external insights into actionable internal plans, manage vendors, ensure compliance, and collaborate cross-functionally to improve screening, diagnosis and patient linkage to care across HIV and viral hepatitis.