Jobs at Gilead Sciences

Lead the national sales organization for HBV and HDV, managing six Regional Directors to drive sales strategy, execution, product launch, performance management, cross-functional alignment, compliance, and leadership development to grow market share and revenue.

Manage global clinical trial material distribution to depots and sites, analyze and mitigate shipment and inventory risks, coordinate with depots/couriers/partners, ensure cGMP/GDP and import/export compliance, support audits and regulatory filings, develop tracking tools and dashboards, drive process and system improvements (ERP/IRT), and mentor junior team members.

Serve as QC lead for late-stage biologics, driving integrated analytical lifecycle strategies (method validation/transfer, specifications, stability, reference standards), providing scientific and regulatory judgment, leading QC input for regulatory submissions, overseeing external labs/CDMOs, mentoring colleagues, and resolving complex technical and compliance issues to support registration and commercialization readiness.

Lead biostatistics for Virology drug programs across discovery, development, and marketed products. Design trials, provide statistical leadership for molecules/indications, support regulatory interactions, oversee analyses and reporting, manage internal/external resources, supervise staff, and contribute to NDA/BLA submissions and departmental strategic initiatives.

Lead end-to-end ownership and delivery of finance and boundary applications (BlackLine, OneSource, SAP-integrated tools, Salesforce PRM). Manage vendors, programs, governance, integrations with SAP S/4HANA, stakeholder alignment, risk/escalation, and continuous improvement across finance systems to ensure compliance, scalability, and high performance.

Lead and operate the cloud-based CRM data replication layer for US Commercial IT. Manage replication pipelines, ensure data integrity, define RPO/RTO, troubleshoot latency/failures, optimize AWS S3 storage and costs, and coordinate with Product Owners, MDM, Analytics, Compliance, and vendor teams to maintain high availability and compliance for downstream integrations.

Lead global commercial strategy for early-stage oncology assets (preclinical through Phase 2). Develop commercially informed Target Product Profiles and clinical strategy input, define disease and portfolio strategies, drive value propositions and access planning, support business development assessments, own commercial workstreams in governance, and align cross-functional partners to maximize patient impact and asset value.

Lead statistical strategy for late‑phase virology clinical programs: design studies, develop analysis plans, interpret results, support regulatory submissions, collaborate cross‑functionally, and potentially serve as Biostatistics Program Lead overseeing internal teams and CRO partners.

Lead and oversee statistical programming for clinical studies: produce analysis datasets, tables/figures/listings, ensure regulatory-compliant documentation and submissions, manage resources, support integrated analyses, and collaborate across clinical development.

Lead and oversee statistical programming for clinical studies, managing design/coding of analysis datasets and outputs (tables/figures/listings), ensuring regulatory-compliant documentation and electronic submissions, coordinating resources and vendors, providing primary/secondary programming support, and implementing strategic initiatives to meet timelines and resolve study issues.

Lead Regulatory Affairs resource management, providing data-driven workforce planning, forecasting, and named resourcing. Oversee Planisware/Smartsheet tooling, drive strategic workforce planning cycles, influence cross-functional stakeholders, manage resourcing-related projects and training, and mature RA resource management capability to align headcount, skills, and vendor strategies with organizational priorities.

Manage end-to-end operational delivery of early-phase oncology clinical trials, coordinating internal teams and CROs/vendors, maintaining timelines and budgets, drafting clinical documents, ensuring regulatory compliance (FDA/EMEA/ICH/GCP), identifying and mitigating risks, and supporting study reporting and scientific communications. Office-based role with required travel.

Lead MDM business ownership, data governance, and operational excellence for commercial data. Prioritize MDM roadmap, drive data quality and standards, and partner with IT and vendors. Enable AI adoption by identifying use cases, piloting solutions, and scaling AI-driven analytics and automation. Serve as a trusted advisor, facilitate governance, define KPIs, and improve processes across stakeholders.

Lead global Finance and Commercial ERP solution delivery, owning R2R, S2S, O2C and commercial operations. Define strategy and roadmap for SAP Finance and Commercial modules, ensure regulatory compliance (GxP, SOX), oversee post-merger ERP harmonization, drive governance, stakeholder alignment, and build a high-performing solutions team to deliver standardized, scalable ERP capabilities.

Lead trade and channel strategy for Gilead US Market Access: define distribution networks, drive channel recommendations, lead RFP/vendor selection, set KPIs, perform primary research and analytics, support contract negotiations, ensure regulatory and audit compliance, and manage/mentor direct reports while collaborating cross-functionally with Brand, Finance, Legal, Government Affairs, and Operations.

Lead strategy and execution for clinical systems and analytics (Veeva, Medidata, Salesforce, cloud platforms). Oversee large technical programs, scalable data architectures, compliance with GxP, cross-functional stakeholder alignment, budgeting, and people leadership to deliver analytics-ready clinical data and drive operational improvements.

Lead FP&A for Global IT and Site Operations, driving strategic planning, annual budgeting, forecasts, capital and OpEx evaluation, monthly/quarterly close, variance analysis, and process improvements. Serve as trusted finance business partner to IT and Site Ops, deliver executive decision support, and lead a high-performing finance team.

Senior finance leader driving financial strategy for oncology and inflammation R&D. Partners with senior stakeholders to provide business-case evaluations, portfolio optimization, valuation frameworks (NPV, risk‑adjusted modeling), governance (SOX, audit‑ready), process automation, and builds a high‑performing Program Finance team to influence development and commercial decisions.

Manage regional clinical trials (typically Phase I or small studies) including study planning, timelines, budgets, CRO/vendor oversight, site oversight, regulatory document review, and cross-functional coordination to ensure compliance and timely data delivery.

Provide strategic and operational statistical leadership for clinical development in Inflammation. Lead statistical planning, sample-size determination, SAP authoring, TFL and CSR review, cross-functional collaboration, regulatory defense, and supervise internal and external teams across multiple clinical trials and departmental initiatives.