Jobs at Gilead Sciences

Leads real-world evidence analysis, programming, data governance, visualization, knowledge management, and business performance reporting within a pharmaceutical medical affairs research organization. Manages budgets, financial planning, risk analysis, operational research, continuous improvement, vendor and cross-functional partnerships, KPI adoption, and analytical training. Oversees data accuracy, compliance, reporting, optimization initiatives, and people management while translating complex data into actionable business insights.

Supports late-stage inflammatory bowel disease clinical development programs, including clinical trial design, protocol and study document preparation, trial execution, data analysis, regulatory submissions, investigator support, and scientific reporting. Collaborates with cross-functional teams, contributes to clinical monitoring and study materials, addresses study obstacles, and ensures compliance with FDA, EMA, ICH, GCP, and company standards.

Develop and operationalize machine learning and statistical solutions for pharmaceutical development and manufacturing. Responsibilities include predictive modeling, computer vision, exploratory analysis, model validation, deployment, monitoring, software package development, testing, documentation, and model governance. The role translates scientific and business challenges into scalable applications, collaborates with multidisciplinary teams, supports AI/ML projects, and communicates findings to scientific and cross-functional stakeholders.

Provides strategic and operational biostatistical leadership for inflammation clinical development programs. Leads study design, sample size determination, protocol development, statistical analysis plans, tables, figures, listings, clinical study reports, publications, and regulatory responses. Collaborates with clinical, safety, regulatory, programming, data management, and project teams; oversees internal and external resources; directs multifunctional teams; develops staff; and supervises personnel.

Drives pharmaceutical sales within an assigned territory by promoting Gilead products to healthcare professionals. Builds relationships with key stakeholders, executes territory business plans, achieves sales targets, manages budgets, interprets market data, and collaborates with Medical, Marketing, and Commercial teams. Provides therapeutic expertise, supports professional events, mentors junior staff, and ensures compliant product promotion.

Leads enterprise technology strategy, architecture, support, and delivery for cell order management and supply chain platforms. Manages analysts, vendors, roadmaps, releases, integrations, incidents, service governance, and operational resilience across Oracle, SAP, Salesforce, and related systems. Partners with business and technology stakeholders to deliver compliant, scalable solutions and measurable value in a regulated life sciences environment.

Represents Gilead’s liver therapeutics portfolio across West Virginia by managing healthcare-provider accounts, developing territory sales plans, educating customers on products and disease states, and achieving sales targets. The role requires pharmaceutical sales expertise, cross-functional collaboration, compliance with promotional and regulatory standards, reporting, territory budget management, and regular travel. Candidates need substantial pharmaceutical, biotech, or healthcare sales experience, a valid driver’s license, and the ability to communicate complex clinical information effectively.

Promote Jyseleca, a JAK inhibitor for rheumatoid arthritis, to healthcare professionals. Achieve sales plans and KPIs, coordinate with co-promotion partners, improve product and positioning understanding, share market insights, execute events, and contribute knowledge and proposals to the inflammation business team.

Manages regional market access and reimbursement activities across Northern Germany. Analyzes healthcare environments, prescription controls, public accounts, and regional contracts; develops and negotiates rebate and selective contracts; and translates market intelligence into commercial strategies. Partners with health insurers, healthcare professionals, authorities, and cross-functional teams, while coaching internal stakeholders and supporting execution of initiatives that improve regional business performance.

Leads regional market access and reimbursement activities across Eastern Germany. Analyzes healthcare policies, prescription controls, contracts, and public account influence; develops commercial strategies, negotiates rebate agreements, and supports execution with cross-functional teams. Builds relationships with health insurers, healthcare organizations, physicians, and professional associations. Coaches internal stakeholders, identifies market opportunities, addresses prescription barriers, and provides market access intelligence to improve regional business performance.

Leads scientific planning, execution, analysis, reporting, and regulatory support for late-stage inflammatory bowel disease clinical development programs. Responsibilities include protocol and study document development, clinical trial implementation and oversight, data analysis, regulatory submissions, investigator support, and coordination across functional teams. Requires relevant biopharmaceutical or drug development experience, knowledge of clinical trial regulations and Good Clinical Practice, and an advanced scientific degree.

Leads biostatistical activities for clinical studies and products, including trial design, statistical analysis plans, regulatory submissions, safety and biomarker analyses, databases, and statistical programming. Provides consultation on methods, endpoints, and results; directs internal and external teams; supports clinical development documentation, publications, SOPs, and special projects. Requires advanced biostatistical expertise, biomedical data analysis experience, SAS proficiency, and experience leading projects and teams.

Leads Kite’s US Integrated Insights organization, partnering with Marketing, Market Access, and commercial leadership. Oversees brand and market access insights, market research, forecasting, launch readiness, performance reporting, business planning, and strategic analytics. The role translates complex market and organizational data into recommendations, drives cross-functional alignment, manages forecasting and commercial KPIs, and develops a high-performing insights team supporting oncology and cell therapy businesses.

Leads Gilead’s Philadelphia/Baltimore HCV and PBC sales region, managing and developing sales specialists, achieving regional targets, building healthcare-provider relationships, and coordinating with marketing, medical, and national account teams. The role requires strategic planning, coaching, product-launch expertise, scientific and pharmaceutical knowledge, compliance oversight, cross-functional project leadership, and regular travel throughout the assigned multi-state territory.

Leads global Regulatory CMC strategy and submissions for autologous CAR-T therapies, including Module 3 content, lifecycle management, change assessments, health authority interactions, and cross-functional coordination across clinical and commercial programs.

Lead Gilead’s global trade compliance program across import/export compliance, customs classification, licensing, sanctions, risk controls, audits, regulatory engagement, and trade optimization. Partner with Legal, Tax, Finance, Supply Chain, and Procurement to align customs processes with financial and tax strategies. Standardize global processes, optimize SAP GTS or equivalent systems, improve reporting, deliver training, and lead a global compliance team.

Leads Medical Affairs strategy and a field-based team across the Northeast, advancing clinical value, market access, and appropriate adoption of cell therapy. Engages payers, treatment centers, and oncology practices to address evidence needs, referral pathways, site readiness, and patient access barriers. Responsibilities include people leadership, strategic planning, budgeting, hiring, team development, cross-functional collaboration, thought-leader engagement, and representing the company with medical and regulatory stakeholders.

Leads GxP audits, inspection readiness, regulatory inspections, and quality compliance activities across Kite R&D operations in the EU and worldwide. Provides GCP and GVP expertise, manages CAPAs, supports annual audit planning, represents the organization with health authorities, and leads quality improvement initiatives. The role also mentors team members, harmonizes global quality practices, and may provide compliance leadership to R&D groups and projects. Travel is expected 30% to 50% of the time.

Associate Counsel will draft, review, negotiate, and advise on contracts supporting Medical Affairs and Clinical Data Science within a pharmaceutical research organization. Responsibilities include managing data, collaboration, vendor, confidentiality, and service agreements; advising on intellectual property, privacy, security, and business risks; resolving escalations and disputes; improving templates and legal processes; and collaborating with cross-functional and international stakeholders.

Provides strategic and scientific leadership for oncology clinical development programs from IND-enabling activities through early development and registration planning. Oversees clinical studies, medical monitoring, protocols, regulatory interactions, cross-functional execution, external stakeholder engagement, scientific presentations, and portfolio planning. The role also mentors physicians and contributes to business development and innovation assessments.