Search the 30 jobs at Gilead Sciences, Inc

The Finance Manager in FP&A will provide a range of financial planning and analysis activities, support business units with financial results, maintain revenue adjustment models, and facilitate operating expense budgets and forecasts.

The Therapeutic Specialist I is responsible for achieving sales targets in a designated territory, training team members, managing budgets, collaborating on projects, addressing market issues, and ensuring compliance with industry regulations.

The Administrative Coordinator for Public Affairs at Gilead will support the team with administrative tasks, manage corporate giving initiatives, oversee the Grants Committee, and ensure effective internal and external communications.

The Senior Manager of Biostatistics will lead biostatistical analysis for NDA submissions, provide statistical consultation on clinical trials, author statistical analysis plans, and oversee statistical activities in collaboration with cross-functional teams to ensure successful project deliverables.

The Therapeutic Specialist HIV is responsible for achieving sales objectives, promoting Gilead's products to healthcare professionals, managing territory budgets, and building relationships with customers. They must prepare business plans, monitor sales progress, and collaborate with internal teams and external partners to enhance product visibility and compliance.

The Senior Manager, Supply Chain will oversee supply planning processes, manage inventory reporting, prepare product updates, and ensure supply chain metrics are met while minimizing risks to patient supply. Collaboration with various teams to optimize results is key.

The Market Access Manager at Gilead will support strategic pricing and reimbursement analyses, develop pricing and reimbursement strategies, and create value propositions for national and local payers, contributing to improved access to therapies for patients with life-threatening diseases.

The Associate Scientist will work in a laboratory setting to optimize large molecule therapeutics through biophysical, biochemical, and functional assays. Responsibilities include the engineering of antibody binding domains, evaluating binding properties of biologics, and collaborating with cross-functional teams to develop novel biologics for clinical use.

The Therapeutic Specialist I is responsible for achieving sales targets in their territory, providing training, monitoring sales progress, and collaborating with external partners. The role requires strong interpersonal skills, a working knowledge of relevant therapeutic areas, and the ability to analyze complex issues and present recommendations.

The Senior Manager of Market Access will lead the strategy and planning for market access in Oncology, manage reimbursement processes, develop pricing strategies, and conduct health economic analyses. The role involves engaging with key stakeholders and cross-functional teams to ensure access to Gilead's products.

As a Senior Therapeutic Specialist, you will represent Gilead products to healthcare professionals, develop business plans for your territory, monitor sales progress, and build relationships with key customers while ensuring compliance with regulations.

The Sr. QA Specialist will collaborate with cross-functional teams to ensure compliance of QC testing with Quality and Regulatory requirements. This involves reviewing and approving test methods, lab investigations, and analytical data while managing audit readiness and continuous improvement initiatives.

The Sr Manager, IT Systems Engineering will maintain and enhance middleware solutions, leading technical discussions and ensuring seamless integration across systems. They are responsible for system performance, disaster recovery planning, and compliance with security regulations. The role involves collaboration with various teams to establish system roadmaps and enhance overall business user satisfaction with IT solutions.

The Senior Manager, Quality for Combination Products at Gilead is responsible for managing compliance and ensuring that the Quality Management System (QMS) meets global regulations for combination products. This role involves monitoring industry standards, participating in audits and inspections, engaging with various stakeholders, and leading improvements in QMS processes to support the development and market advancement of combination products.

The Therapeutic Specialist will drive growth for Gilead's Liver and Invasive Antifungal Infections treatments in designated regions. Responsibilities include promoting products to healthcare professionals, preparing account plans, achieving sales targets, and building relationships with key customers while ensuring compliance with regulations.

Responsible for achieving sales targets and coverage in assigned territory, collaborating with team members, and contributing to regional training while documenting and measuring performance.

The Senior Research Associate II will play a key role in drug discovery for Virology, Oncology, and Inflammation by engineering, expressing, purifying, and characterizing proteins. They will handle protein quality assessments using biophysical analytics and collaborate with cross-functional teams to present results.

The Manager of Quality Systems is responsible for enhancing and integrating Quality Systems, documenting QA projects, managing stakeholder relationships, and ensuring project performance and risk management throughout the project lifecycle. The role includes guiding junior staff and staying updated on industry trends to improve QA processes.

The Quality Assurance Operations Specialist II interacts with contract manufacturers to resolve quality issues and ensures compliance with regulatory requirements. They participate in developing SOPs, maintain quality programs, review production documents, and lead investigations related to quality control. This role requires strong knowledge of quality systems and an ability to work independently and collaboratively within teams.

The Sr. Manager, Biostatistics will lead biostatistical analysis for clinical studies, provide statistical consultation, and support NDA submissions. Responsibilities include overseeing statistical activities, participating in clinical development planning, and contributing to trial design discussions.