Gilead Sciences

Director

• Handle quantitative analyses in the Oncology, Inflammation and Virology Therapeutic Areas of Gilead Sciences, Inc.
• Responsible for the conduct as well as interpretation and reporting of the analyses, and support of regulatory filings
• Champion model-informed drug development (MIDD) across drug discovery and development
• Serve as a subject matter expert for modeling and simulation to cross-functional partners
• Leading quantitative and innovative strategies within clinical pharmacology to impact MIDD during the life cycle of the program
• Evaluate and apply strategy and content as appropriate
• Guide dose regimen/optimization strategies in partnership with other therapeutic area leads and clinical pharmacology leads to enable data-driven decisions
• Develop high-quality modeling and simulation strategy and content: author/review/approve modeling and simulation analysis plans and outputs, interpretation, and presentation of key findings to regulators and to stakeholders as needed
• Ensure adherence to agreed timelines and budgets to ensure prompt and accurate execution of deliverables from clinical pharmacology studies and programs
• Develop and present training within and outside the department as needed

Clinical Pharmacology Associate Director

• translate global supply strategies into an integrated, feasible, and optimized master production schedule (MPS).
• act as primary conduit between Global Network Planning and Site Supply Chain Planning.
• govern planning outside and inside the 4‑month planning time fence.
• drive proactive risk mitigation in the 6–24‑month horizon.
• maintain governance for all plan changes within the 4‑month frozen window.
• lead scenario modeling and recommend adjustments in response to supply risks, capacity shifts, regulatory changes, and demand variability.
• support lifecycle readiness including artwork changes, regulatory updates, tech transfers, and market expansions.
• track and report KPIs including MPS attainment, schedule adherence across internal and external nodes, capacity utilization, and supply reliability/OTIF.

Associate Director, Master Production Planner

• Responsible for translating global supply strategies into an integrated, feasible, and optimized master production schedule (MPS) across the internal and external manufacturing network.
• Acts as the primary conduit between Global Network Planning and Site Supply Chain Planning, ensuring alignment on feasibility, constraints, and assumptions.
• Owns and governs the 24-month master production schedule for DS, DP, and FG across internal and external manufacturing nodes.
• Provides long-range planning and integrates global strategies into forward-looking production plans.
• Maintains governance for all plan changes within the 4-month frozen window.

Associate Director – Master Production Planner

• Provide Statistical leadership to late-stage oncology clinical trials: developing trial design options and providing high quality decision support.
• Statistical lead for a specific oncology molecule/indication in Health Authority interactions and maintain an accountability thread to TA head
• Works collaboratively with Statistical Programmers, Biostatisticians, Clinical Research Associates, Clinical Data Managers and other Clinical, Global Drug Safety, Regulatory and Project Management staff to meet project deliverables and timelines for statistical data analysis and reporting
• Directs internal and external teams across multifunctional project or functional areas, leads initiatives to gather, organize, and analyze data from different sources such as virology, Case Report Forms, and patient tracking, works with management and Human Resources to satisfy short-term staffing needs, defends statistical aspects with regulatory agencies, develops staff capabilities, and recognizes/rewards desired performance
• Is expected to oversee and contribute to the completion of all technical and operational statistical activities for a group of clinical trials for a compound/indication or equivalent through management of internal and external resources
• Leads two or more components of departmental strategic initiatives

Director, Biostatistics

• Handle quantitative analyses in the Oncology, Inflammation and Virology Therapeutic Areas of Gilead Sciences, Inc.
• Responsible for the conduct as well as interpretation and reporting of the analyses, and support of regulatory filings.
• Champion model-informed drug development (MIDD) across drug discovery and development and serve as a subject matter expert for modeling and simulation to cross-functional partners.
• Leading quantitative and innovative strategies within clinical pharmacology to impact MIDD during the life cycle of the program.
• Evaluate and apply state-of-the-art quantitative pharmacology approaches for clinical pharmacology decision-making and for global regulatory submissions, including INDs, IBs, NDAs, BLAs, MAAs, and pediatric plans in collaboration with key stakeholders.
• Guide dose regimen/optimization strategies in partnership with other therapeutic area leads and clinical pharmacology leads to enable data-driven decisions.
• Develop high-quality modeling and simulation strategy and content: author/review/approve modeling and simulation analysis plans and outputs, interpretation, and presentation of key findings to regulators and to stakeholders as needed.
• Ensure adherence to agreed timelines and budgets to ensure prompt and accurate execution of deliverables from clinical pharmacology studies and programs.
• Develop and present training within and outside the department as needed.

• Accountable for the global strategy, governance, and long-term performance of Stability Program Management and Reference Standards & Analytical Controls across Gilead’s development and commercial portfolio.
• Define and own the enterprise-wide strategy, vision, and multi‑year roadmap for Stability Program Management and Reference Standards & Analytical Controls.
• Design, own, and maintain global policies, standards, procedures, governance models, and decision frameworks.
• Serve as the final global authority for interpretation, application, and risk-based decision-making related to Stability and Reference Materials processes.
• Oversee and direct global implementation strategies for new or revised processes.
• Sponsor development of training frameworks, role-based enablement, certification expectations, and change management approaches.
• Define, monitor, and govern enterprise-level KPIs and performance indicators for Stability and Reference Materials.
• Act as the global process authority during regulatory inspections and health authority interactions.
• Lead continuous improvement and change management, applying Lean principles to process design and execution.
• Lead and sustain a global, matrixed network of senior SMEs and functional leaders, influencing without direct authority.

Director, Quality Control – Stability and Reference Materials

• develop and execute proactive, integrated public affairs communication strategies and content that articulate and support Gilead’s legislative, regulatory and public policy objectives
• translate complex policy topics into accessible, persuasive narratives for external audiences
• monitor and synthesize public affairs developments to inform proactive communication planning
• identify opportunities, venues and creative communications tactics to meet Gilead’s objectives
• strengthen message discipline, ensuring alignment across Public Affairs, Government Affairs, Legal, and functional partners
• advise senior leaders and internal partners on best practices and creative ways of communicating and activating campaigns
• ensure Public Affairs communication efforts complement Government Affairs’ policy, trade, and coalition building strategies
• support the development of content for policymakers, advocacy groups, NGOs, and external experts
• partner with enterprise communicators to ensure consistency across therapeutic, corporate, and reputation driving messaging
• support issue monitoring and response related to emerging risks and evolving narratives that may impact Gilead’s reputation.

Sr Director, Public Affairs, External Affairs

Community Manager

• Lead on all community-related initiatives and is fully responsible for augmenting regional sales of Gilead's HIV franchise within targeted markets.
• Collaborate with Sales & Marketing.
• Focus on the timely delivery of complex clinical information on the treatment and prevention of HIV and the role of Gilead products in the treatment and prevention of this disease to culturally diverse patient populations, allied healthcare providers, and high-level decision-makers.
• Responsible for establishing strong working partnerships with key institutions and organizations serving these communities.
• Facilitate linkages from these institutions, organizations, and professionals to underserved patients to improve access to care and treatment for HIV.

Community Liaison

• provide strategic and operational statistical leadership for clinical development programs
• represent Biostatistics at study management team and development team for multiple studies or programs
• collaborate closely with Clinical Development, Patient Safety, Clinical Pharmacology, Regulatory Affairs, Project Management, Programming, Clinical Data Management
• serve as lead statistician for Phase 1–3 clinical trials
• advise internal and external partners on statistical analysis strategies

Associate Director, Biostatistics

• Provide Statistical leadership to Virology clinical trials: developing trial design options and providing high quality decision support.
• Statistical lead for a specific Virology molecule/indication in Health Authority interactions and maintain an accountability thread to TA head
• Works collaboratively with Statistical Programming, Biostatistics, Clinical Research, Clinical Data Management, Global Drug Safety, Regulatory and Project Management management/staff to meet project deliverables and timelines for statistical data analysis and reporting.
• Uses knowledge of Regulatory requirements regarding statistical principles to ensure the company meets its Regulatory, scientific, and business objectives.
• Collaborates with study investigators, outside experts, and internal colleagues to present and publish trial results and statistical analyses within and outside of the company.
• Negotiates project timelines given constraints, works with senior management and Human Resources to identify long-term staffing plans, provides career development opportunities to staff, and participates in strategic risk assessment based on statistical analyses or principles.
• Expected to oversee and contribute to the completion of all technical and operational statistical activities for multiple development programs for a compound or equivalent through management of internal and external resources.
• Provides overall leadership for a departmental strategic initiative with experience directly supervising personnel.

• Lead the development and implementation of global HEOR strategies and programs to support marketed HIV products and pipeline assets.
• Serve as a strategic partner across functions, including clinical development, marketing, medical affairs, government affairs, and market access, to support commercialization and lifecycle planning.
• Partner with cross‑functional stakeholders to develop and support robust product value propositions that optimize access, reimbursement, and uptake.
• Identify global HEOR evidence needs and gaps; design, conduct, and deliver studies, models, and tools to support value demonstration and product differentiation for assigned indications.
• Provide HEOR input into clinical development programs to ensure evidence generation aligns with payer and health system requirements.
• Collaborate with the HEOR Center of Excellence to support the development and execution of patient‑reported outcome (PRO) strategies.
• Maintain current knowledge of evolving regulatory, reimbursement, and policy landscapes and cultivate external research relationships with HEOR key opinion leaders.
• Disseminate HEOR data and study results through appropriate internal and external channels in compliance with applicable policies and regulations.

Director, Global Value and Access, HIV

Compliance

• Partner across the Office of Ethics and Compliance, Legal, and other cross-functional teams to support the delivery of Global Compliance initiatives and program enhancements across multiple geographies, including the U.S.
• Translate defined compliance priorities into clear project plans, including scope, timelines, milestones, dependencies, and deliverables, and support execution through completion.
• Coordinate execution of Global Compliance support across stakeholders, tracking progress, identifying risks or issues, and helping teams stay aligned and on track
• Support implementation of assigned initiatives in line with established ethical standards, governance expectations, and operational requirements
• Provide hands-on operational support for core compliance activities, including initial triage of inquiries received through Global Compliance-supported intake channels, such as Conflict-of-Interest disclosures, ensuring timely routing, prioritization, and coordination with appropriate subject-matter owners
• Support the deployment and adoption of new or updated compliance tools, platforms, or processes across geographies
• Contribute to change management efforts by helping develop communications, guidance, and practical resources to support adoption and consistent use of compliance frameworks, tools, and processes
• Maintain execution tracking for assigned initiatives and operational activities, including milestones, dependencies, risks, and issues
• Prepare clear, concise status updates, summaries, and materials for compliance leadership, highlighting progress, key decisions, risks, and recommended actions
• Support leadership discussions by synthesizing information across projects and identifying themes or cross-cutting issues
• Identify recurring execution challenges or inefficiencies across compliance operations (e.g., intake management, project handoffs, or resource adoption)
• Propose and help implement practical improvements to processes, ways of working, or governance to enhance efficiency, consistency, and user experience
• Contribute to knowledge-sharing efforts by helping document and disseminate best practices, lessons learned, and operational insights across the organization.

Senior Manager, Compliance Excellence and Innovation Partners

Events

• Build strong relationships and engage healthcare providers across various touchpoints
• Develop and execute a comprehensive territory business plan that meets customer needs and achieves sales goals
• Maintain a deep understanding of Gilead's products, competitive products, and the complexities associated with the therapeutic area’s disease state
• Actively promote the appropriate use of Gilead products to healthcare professionals
• Partner effectively with local cross-functional colleagues to ensure a seamless customer experience
• Demonstrate the ability to build and maintain strong internal and external working relationships
• Model and uphold Gilead's compliance standards and ethical behavior
• Leverage advanced influencing and relationship skills to drive sales outcomes
• Build solid relationships and establish long-term partnerships with healthcare providers

Senior Therapeutic Specialist, HIV Prevention

• Provides input into product development strategies and/or research or clinical development plans for assigned products/projects
• Authors the clinical pharmacology plan for one or more products in the assigned disease or therapeutic area
• Leads and manages design and conduct of clinical pharmacology studies
• Designs clinical pharmacology study protocols, study data analysis, modeling and simulation plans
• Works with cross-functional partners and study sites to implement and monitor clinical pharmacology studies
• Analyzes, interprets and authors documents for clinical and regulatory submissions

Associate Clinical Pharmacology Director

• Partner with the LL lead on key projects
• Collaborate with Clinical Development, HEOR, Market Access, Government Affairs, Marketing
• Execute on tactics like advisory boards and publications
• Drive the development and execution of the cross-functional product and disease strategy
• Provide guidance for the disease strategy and cross-functional projects
• Maintain a thought leader network and collaborate with other functional areas

Clinical Pharmacology Associate Director

Associate Director, Master Production Planner

Associate Director – Master Production Planner

Director, Biostatistics

Clinical Pharmacology Associate Director

Director, Quality Control – Stability and Reference Materials

Sr Director, Public Affairs, External Affairs

Community Liaison

Associate Director, Biostatistics

Director, Biostatistics

Director, Global Value and Access, HIV

Senior Manager, Compliance Excellence and Innovation Partners

Senior Therapeutic Specialist, HIV Prevention

Associate Clinical Pharmacology Director

Assoc Director, Medical Affairs