Jobs at Gilead Sciences

The Director of Commercial Product Strategy will oversee the execution of the global commercial strategy for BIKTARVY in Mid-Size markets, ensuring alignment and effective rollout. The role includes advising on key business topics, facilitating cross-functional collaboration, and supporting local market needs.

The Clinical Trials Manager oversees Phase I-IV trials, manages budgets, collaborates with teams, and ensures compliance with regulations while driving study efficiency.

Lead the Government Affairs team and develop strategies to enhance Gilead's agenda in the UK and Ireland. Collaborate with stakeholders, policymakers, and internal teams to influence health policies and advance Gilead's interests.

The Senior Manager, IT will oversee AI product delivery, manage MLOps pipelines, and collaborate with stakeholders to ensure the implementation of AI solutions for commercial applications.

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

The Director of Public Affairs will lead strategic communication programs, manage media relations, and coordinate with stakeholders to promote Gilead's initiatives, particularly in HIV-related areas.

The Senior Director will lead commercial insights, support executive decisions, manage a global team, and drive strategic initiatives for market success.

The Executive Director will lead public affairs strategies for Gilead's Intercontinental Region, focusing on communications, advocacy, and stakeholder engagement to improve health outcomes. Responsibilities include strategy execution, stakeholder engagement, team leadership, and budget oversight.

The Associate Director manages Gilead's Global Meetings strategy, oversees event planning, collaborates with various stakeholders, and leads team members.

The Director of GV&A HIV Execution leads market access strategies for HIV products in ICR markets, partnering with cross-functional teams, stakeholders, and market affiliates to optimize access and reimbursement while implementing new capabilities and monitoring KPIs.

Lead GxP audits, manage audit activities, ensure compliance, develop CAPAs, support inspections, and promote a quality culture in R&D.

The Sr. CTM Associate supports global clinical trial operations, ensures compliance with protocols and regulations, assists with vendor management, and communicates across functional teams to manage study activities effectively.