Search the 74 jobs at Gilead Sciences, Inc

The Sr. Specialist in PRC Operations will manage the review and approval of promotional materials, ensuring quality standards and timeline adherence. Responsibilities include facilitating meetings, providing training, overseeing electronic review cycles, collaborating with various stakeholders on product launches and initiatives, and supporting operational excellence.

The Senior Quality Engineer will oversee quality assurance for medical device combination products, focusing on compliance with regulations and standards. Responsibilities include collaborating on product development, managing quality improvement initiatives, and addressing complex technical issues. Candidates need a strong background in quality systems and experience in medical device regulations.

As Senior Manager of ACE Insights & Analytics, you will lead market research and forecasting for the ACE region focusing on CAR T cell therapy in Oncology. You will track product performance, develop insights for decision making, and collaborate with cross-functional teams to ensure effective market strategy. Your role includes managing analytics solutions, reporting on KPIs, and communicating findings to senior leadership.

The RTR Intercompany Accountant will manage intercompany accounting activities including processing cross charge transactions, reconciling intercompany accounts, preparing accruals, and interacting with local finance teams while adhering to company policies and procedures.

As a Public Affairs Specialist I and Grant Administrator at Gilead, you will manage corporate giving strategies, oversee grant and donation programs, and ensure compliance across various departments. Responsibilities include coordinating meetings, supporting communication initiatives, and assisting with budget management. Strong project management skills and ability to manage multiple stakeholders are essential.

The Qualified Person will ensure compliance with regulations, release medicinal products, and maintain quality assurance standards. Key responsibilities include certifying batches, approving quality reviews, participating in compliance audits, and collaborating with various teams to uphold quality objectives in pharmaceutical development.

The Digital Marketing Operations Manager will oversee the implementation and optimization of the HCP Portal and other digital projects, ensuring compliance with regulations while improving customer experience and tracking digital campaigns. They will also serve as a local expert coordinating with global teams and training sales teams on digital tools.

The Therapeutic Specialist I is responsible for achieving sales targets and building relationships with healthcare professionals in assigned territories. They monitor sales progress, manage territory budgets, and collaborate with internal teams while ensuring compliance with regulatory standards.

The Therapeutic Specialist I is responsible for achieving sales and frequency targets in a designated territory, collaborating with cross-function teams, engaging with customers at events, and managing budgets. This role also involves training team members, monitoring sales progress, and ensuring compliance with industry regulations.

As a Therapeutic Specialist at Gilead, you will represent and promote products to healthcare professionals, manage territory business plans, develop key relationships, and ensure compliance with company guidelines. You're expected to meet sales targets and support their mission of improving patient lives through effective communication and education.

The Administrative Coordinator provides essential administrative support to the Global Trade Operations team, assisting with budget tracking, scheduling meetings, organizing events, and supporting new hires. This role requires proficiency in Microsoft Office and adaptability to dynamically support team objectives.

The Legal Coordinator will assist the Filing & Formalities team in preparing and managing documentation related to Intellectual Property, including obtaining signatures and filing applications. The role requires strong organizational and communication skills, along with relevant experience in IP law or paralegal work.

The Senior Manager, Project Management at Gilead is responsible for planning and executing multiple CMC programs, collaborating with cross-functional teams, managing program risks, and leading department initiatives. This role requires a strong understanding of drug development processes and proficiency in project management tools.

The Senior Manager, R&D Information Systems will lead the Reporting Center of Excellence, manage the Vault and ComplianceWire reporting systems, facilitate training sessions, validate reports, harmonize master data, and collaborate with various stakeholders for optimizing data management.

The Sr Manager, IT Systems Engineering will enhance and maintain middleware solutions, lead technical discussions on integrations, ensure system performance and compliance with regulations, manage disaster recovery plans, and collaborate with various stakeholders in a fast-paced pharmaceutical IT environment.

The Therapeutic Specialist I is responsible for achieving sales targets in their territory by building relationships with healthcare professionals, promoting Gilead's products, and collaborating with cross-functional teams. This role includes territory management, training, and performing administrative tasks related to sales progress and compliance with regulations.

The (Senior) Product Manager for Virology at Gilead will lead projects and support marketing plans, collaborating with various departments to achieve revenue goals. Responsibilities include project management, market research, developing brand strategies, ensuring compliance, and managing multi-channel activities to strengthen Gilead's role in virology.

The Senior Manager, Market Access will develop and implement market access activities, support pricing governance, and lead strategic initiatives to maximize commercial potential in Australia and New Zealand while collaborating with cross-functional teams and managing external relationships.

The Patent Analyst II will perform Freedom to Operate and Patentability searches, attending R&D project meetings and collaborating with IP attorneys. Key responsibilities include researching, analyzing, and presenting data related to patent filings and scientific inquiries using various chemical and patent databases.

The Senior Research Associate will execute and support the development of analytical methods, perform data interpretation, contribute to method development reports, assist in troubleshooting, and maintain documentation of experimental plans. They will work independently and collaboratively on method development tasks while participating in team meetings and presentations.