Jobs at Gilead Sciences

Leads field-based regional marketing for hematology and oncology therapies, building relationships with healthcare and opinion leaders, gathering market insights, shaping brand strategies, and executing educational programs, advisory boards, conferences, and speaker activities. Partners cross-functionally with sales, marketing, medical affairs, and congress strategy teams to advance adoption of Kite therapies while maintaining compliance with legal and regulatory requirements. Requires extensive regional travel and people leadership.

Leads FP&A for Corporate Affairs, Legal, Compliance, Corporate Responsibility, and Corporate Jets. Responsibilities include long-range planning, budgeting, forecasting, scenario analysis, financial consolidation, management reporting, performance analysis, executive presentations, financial modeling, close support, process and system improvements, governance, controls, and strategic decision support. Partners with senior leaders and manages high-priority analyses while leading teams and driving continuous improvement.

Leads Gilead Germany’s Government Affairs function, managing a team and high-level relationships with federal, state, legislative, regulatory, and policy stakeholders. Develops and executes pharmaceutical policy and advocacy strategies, monitors legislation, advises leadership, and advances market access for innovative therapies. The role focuses on shaping Germany’s pharmaceutical strategy, AMNOG reforms, oncology and cell therapy evidence requirements, and policies affecting HIV and hepatitis treatments. Requires strong government affairs leadership, German healthcare policy expertise, stakeholder influence, strategic judgment, and fluency in German and English.

Leads US payer and value marketing strategy across Kite’s cell therapy portfolio. Oversees payer-facing value stories, economic resources, budget impact models, access tools, and educational materials. Partners with HEOR, Medical Affairs, Brand, Pricing, Contracting, Legal, Regulatory, and field teams to translate evidence into compliant access strategies. Monitors payer dynamics, establishes performance metrics, manages budgets and agencies, and leads a team supporting portfolio and product-specific initiatives.

Performs pharmaceutical quality assurance activities in a GMP- and GLP-regulated environment. Responsibilities include deviation and CAPA review, investigations, root cause analysis, shopfloor QA support, SOP development, audit and inspection support, documentation review, and cross-functional quality projects. The role also mentors junior staff and coordinates complex assignments related to manufactured products and regulatory compliance.

Leads Japan’s CRM strategy, business analysis, and transformation agenda across Veeva CRM, Salesforce, and Veeva Vault CRM. Partners with Commercial, Sales, Marketing, Medical Affairs, and global IT teams to define roadmaps, requirements, solution designs, migrations, testing, deployment, governance, data readiness, and value realization. Oversees vendors, system integrators, operational support, compliance, change management, user adoption, and AI-enabled commercial engagement initiatives.

Leads complex, cross-functional strategic projects across Research to improve organizational effectiveness, collaboration, scientific operations, governance, communications, talent initiatives, and decision-making. Partners with scientific and functional leaders to align priorities, manage stakeholders, risks, timelines, and deliverables, and translate complex scientific and business needs into actionable plans and measurable outcomes. Supports change management, research-wide communications, employee engagement, and collaboration with Informatics, IT, and business teams.

Leads data engineering and AI platform delivery for enterprise operations. Designs scalable AWS and Databricks architectures, builds ELT pipelines with Airflow, develops data models, and establishes governance, security, quality, monitoring, and compliance controls. Partners with stakeholders to translate business needs into production solutions, guides platform evolution, and supports AI-powered automation, agentic architectures, and enterprise integrations. Provides technical leadership and subject-matter expertise across data, analytics, and AI initiatives.

Leads oncology biostatistics for late-stage clinical development, providing statistical strategy for Phase 3 trials, regulatory interactions, submissions, and HTA/commercial evaluations. Manages and develops teams of statisticians, oversees staffing and succession planning, partners cross-functionally on analyses and clinical reports, and applies statistical and regulatory expertise to development decisions. Builds scientific and regulatory networks while driving collaboration, execution, and organizational excellence.

Provides statistical leadership for drug development programs, including translational study design, analysis plans, clinical and biomarker analyses, predictive modeling, regulatory submissions, and technical reports. Collaborates with scientists, clinicians, vendors, and cross-functional teams while overseeing project progress, resources, and deliverable quality. The role requires expertise in clinical trial design, drug development, regulatory principles, immuno-oncology, and SAS or R.

Leads government affairs strategy across Saudi Arabia and GCC markets for Gilead. Shapes healthcare, pharmaceutical access, reimbursement, innovation, and public health policy; advises regional leadership; builds relationships with government and healthcare stakeholders; monitors political and regulatory developments; supports market access, launches, localization, and healthcare transformation; and leads cross-functional policy initiatives and external partnerships.

Leads commercial learning and development for assigned pharmaceutical business units. Partners strategically with stakeholders to identify capability needs, develop training strategies, design curricula and learning journeys, deliver sales training, manage learning roadmaps, implement change initiatives, and measure impact. Builds blended, digital, AI-enabled, and on-the-job learning solutions aligned with launches, portfolio evolution, and organizational goals.

Designs, evaluates, and implements secure enterprise technology solutions across Windows, Linux, databases, cloud, containers, and infrastructure platforms. Partners with business stakeholders, IT teams, security groups, and vendors to translate requirements into scalable architectures. Creates architecture and data-flow documentation, supports hybrid cloud and production transitions, evaluates resiliency and disaster recovery, and contributes to automation, troubleshooting, standardization, and operational excellence in complex manufacturing and quality environments.

Develop and execute HIV pharmaceutical marketing and promotional programs in China. Partner with medical, sales, public affairs, agencies, suppliers, and other cross-functional teams to implement and evaluate campaigns. Manage promotional materials, stakeholder engagement, competitor intelligence, and multiple projects while analyzing sales and marketing data to support continued product growth and market leadership.

Provides clinical oversight and medical monitoring for clinical trials in neurology and autoimmune disease. Supports study design, protocol development, safety review, regulatory submissions, investigator engagement, data interpretation, and clinical development planning. Partners cross-functionally with Regulatory Affairs, Clinical Operations, Safety, Biometrics, Medical Writing, and other teams. The role may also contribute to publications, scientific presentations, advisory boards, due diligence, and external stakeholder engagement.

Manages regulated hazardous waste, environmental compliance, permits, reporting, audits, inspections, training, and EH&S management systems. Conducts hazard assessments, investigates incidents, recommends corrective actions, supports ISO 14001 and ISO 45001 programs, tracks compliance metrics, and collaborates with regulators, vendors, contractors, scientists, and internal stakeholders. Participates in emergency response activities and provides EH&S guidance for operational changes and cross-functional projects.

Represents and promotes Gilead’s HCV products to healthcare professionals across Iowa and Western Illinois. Builds healthcare-provider relationships, delivers clinical and disease-awareness information, develops territory business plans, achieves sales targets, manages budgets, reports adverse events, and maintains regulatory compliance. Requires extensive pharmaceutical or healthcare sales experience, strong influencing skills, regular territory travel, a valid driver’s license, and two overnight stays per week.

Leads oncology key-account strategy across West Florida integrated customers, including major cancer centers and health systems. Builds executive, pharmacy, pathway, and P&T relationships; drives product access, demand, contract pull-through, and protocol placement. Develops cross-functional account and launch plans with Sales, Medical, Marketing, Managed Markets, Contracting, HEOR, and Value Access teams. Provides clinical and product information, manages strategic accounts, and travels regularly to customer sites.

Leads strategic account management and market access for Gilead’s oncology portfolio across Northeast integrated customers. Builds relationships with cancer centers, executives, pharmacy leaders, prescribers, and P&T committees; develops account plans, drives contract pull-through, supports product launches, and coordinates Sales, Medical, Marketing, Managed Markets, Contracting, HEOR, and Value Access teams. Provides clinical and product information, identifies influencers, and expands oncology product access and utilization.

Leads business process optimization and digital enablement for CMC Regulatory Affairs. Responsibilities include process mapping, KPI development, regulatory systems and data improvement, automation and AI initiatives, cross-functional project delivery, change management, business requirements, dashboards, and implementation of technology-enabled solutions across pharmaceutical regulatory operations.