Gilead Sciences

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, such as AIDS Service/Community-Based Organizations (ASOs/CBOs), FQHCs, STI clinics, Addiction/Methadone Clinics, Faith-Based Organizations, cultural/ethnic organizations, and specialty and community pharmacies.
• Facilitate linkages from these institutions, organizations, and professionals to underserved patients to improve access to care and treatment for HIV.
• The successful CL will possess the business acumen and professionalism required to gain the respect of community constituents while being skilled and adept at working with internal and external cross-functional teams in developing strategies and tactical objectives designed to increase product growth in untapped, underserved markets.

Senior Community Liaison

Manager

• Participate in the development and maintenance of global clinical data standards
• Manage work assignments to ensure timely delivery of global library objects
• Support and participate in the Standards Core Committee (SCC)
• Document meeting minutes and other discussions
• Build, maintain, and document the Medidata Rave global library standard objects
• Communicate and reinforce content and interpretation of Kite data standards to project and study teams
• Independently identify and propose process improvements

Manager, Clinical Programming – Clinical Data Standards Management

• May have direct responsibility for supervising and training clinical programmers in the performance of their duties
• Management of programming deliverables in coordination with internal and external cross functional teams
• Perform the execution of programming activities (eCRF and EDC database, integrations, and module connections) for multiple studies of increased complexity and across indications/therapeutic areas
• Provide input into the SOW activities for vendors
• Perform the development and maintenance (migration) of eCRF and EDC database, integrations (e.g., IxRS) and module connections (e.g., Safety Gateway Configuration) based on the protocol and Kite standards
• Oversee creation of operational metadata (including CRF and external) ensuring compliant to Kite standards
• Provide oversight for programming activities which are outsourced to a CRO/Vendor
• Ensure across studies consistency and adherence to standards and governance
• Support Data Review activities (e.g., Review Data Review Plan, develop reporting tool reports, validate reports)
• Perform support of snapshot, database lock activities and deliverables restriction
• Develop, assess, and monitor project priorities/timelines for programming deliverables
• Participate in study team meetings and provide technical expertise with database and reporting applications (e.g., EDC, Tableau, J-Review, Business Objects) and support as needed
• Routinely interface with cross-functional team members
• Ensure that SOPs are properly followed, and documentation is available
• Align with EDC vendor regarding system updates, EDC platform integrations, and issue resolution
• Ensure following programming best practices
• Resolve problems as they arise within defined procedures and escalate, if necessary, at appropriate time
• Represent as internal team leader who decides best course of action
• Participate in CDM, Programming and cross-functional initiatives
• Participate for programming activities during internal audits as well as Health Authority audits
• Align with the department and company strategy and model
• Flexible to changing priorities, detail-oriented, works well under pressure and able to take on unfamiliar tasks.
• Prioritize and delegate, if applicable, effectively study and initiative responsibilities
• Prepare for expanded scope of responsibility with respect to volume and complexity of clinical project work as well as direct report responsibility
• Work collaboratively with Programming (Clinical and Statistical) Clinical Operations, Biostatistics and others study team members to meet project deliverables and timelines.
• Build networks to achieve influence with other functions and represent as Programming technical expert
• Participate in department and/or cross-functional process improvement initiatives as well as special projects and create efficiencies within programming processes
• Participate in review, approve and train on department procedures including SOPs and Working Practices
• Actively Participate in programming team meetings when appropriate.

Manager, Clinical Programming – EDC

Solutions Engineer

• Architect, design, and deliver AWS cloud-native solutions across AI/ML capabilities and enterprise business applications
• Lead the implementation of Generative AI solutions, including retrieval-augmented generation (RAG), agentic workflows, and LLM-integrated systems
• Drive adoption of AI-augmented development practices, including design acceleration, code generation and review, test automation, and debugging
• Serve as the primary technical authority for assigned capabilities, making architectural decisions across APIs, data platforms, frontend, infrastructure, and AI tooling
• Lead technical delivery across onshore and offshore contractor teams, ensuring predictable planning, execution quality, and delivery outcomes
• Mentor and coach engineers through hands-on guidance, pair programming, code reviews, and knowledge sharing
• Partner with data science, business, quality, and regulatory stakeholders to align architecture and delivery with program milestones and compliance needs
• Prototype and validate new capabilities, particularly Generative AI features, to reduce risk before broader team investment
• Define and execute a technical roadmap aligned with business priorities and R&D Information Systems strategy
• Oversee production reliability, operational support, and continuous improvement across DevOps and engineering practices

Senior Architect, Intelligent Solutions Engineering

Marketing

• Lead development, execution, and training of all payer-facing tools and resources
• Partner with Health Economics & Outcomes Research (HEOR) and Market Access teams to create cost-effectiveness evidence aligned with payer needs
• Translate clinical and economic data into clear, compelling value propositions for payer audiences
• Oversee the agency of record to ensure timely delivery of high-quality, on-brand, and compliant material
• Manage annual payer marketing budgets and SOWs
• Work closely with Market Access, Brand Marketing, Medical Affairs, GACO and Account Teams to align payer strategies with overall business objectives

Associate Director, Payer Marketing

• Act as a technical lead for the US Value & Access team and will report to the Value & Access IT Director.
• Support and liaise with a broad team including Market Access Operations, US Commercial Legal, Internal Audit, IT Vendor Management, IT Risk & Controls, and Finance.
• Infuse forward thinking and innovative approaches to building and implementing technologies that support our business as we scale.
• Be the go-to person for all Value & Access IT operational needs – from onboarding new team members, overseeing managed services providers to owning the IT processes that support our technical day-to-day operations.
• Involved from the inception of IT solution ideas through to successful execution of these technology initiatives.
• Projects may include enhancement of existing Revenue Management tools (Model N system modules), system security assessment of third-party SaaS solutions, and implementation of new technologies to enhance business effectiveness.
• Provide new technology project support and oversee the day-to-day operations of our US-based Value & Access systems.

Senior Manager, IT Business Analysis

Director

• Direct internal and external teams across multifunctional projects or functional areas
• Lead initiatives to gather, organize, and analyze data from different sources
• Work collaboratively with Statistical Programmers, Biostatisticians, Clinical Research Associates, Clinical Data Managers and other Clinical, Global Drug Safety, Regulatory and Project Management staff
• Oversee and contribute to the completion of all technical and operational statistical activities for a group of clinical trials
• Lead two or more components of departmental strategic initiatives
• Anticipate obstacles and difficulties of clients and act to meet goals

Associate Director, Biostatistics

• Lead the design, development, and scaling of omnichannel data sciences capabilities—including sales, content and engagement machine learning (ML) models, content‑ranking systems, and engagement prediction frameworks—to support data‑informed commercial decision making
• Establish sustainable, reproducible methodologies for building and deploying data science solutions, ensuring long‑term maintainability and alignment with enterprise architecture and commercial strategy
• Partner with Marketing Science measurement teams to incorporate analytical feedback, performance insights, and validation results into model enhancements and roadmap evolution
• Conduct functional feasibility assessments for omnichannel solution development and collaborate with IT and Commercial Operations on providing business enhancements for CRM, SFMC and Model Monitoring solutions

Associate Director, Marketing Sciences

• Lead and manage a team of direct reports, including hiring and developing diverse top talent.
• Collaborate with Statistical Programming, Biostatistics, Clinical Research, Global Drug Safety, and Project Management to meet project deliverables.
• Ensure adherence to regulatory requirements regarding statistical principles and objectives.
• Negotiate project timelines and manage staffing plans.
• Oversee and contribute to completion of all technical and operational statistical activities for multiple development programs.
• Provide overall leadership for departmental strategic initiatives.

Director, Biostatistics

Artificial Intelligence

• lead the strategy, development, and execution of advanced technology solutions, particularly AI-driven tools
• partner closely with colleagues across legal and compliance, and cross-functional stakeholders
• drive the strategic roadmap for AI and automation in support of core ethics and compliance activities
• oversee the lifecycle management of ethics and compliance systems and platforms, ensuring integration, data quality, usability, and sustainability

Director, Global Compliance Systems – AI Enablement

Supply Chain

• Act as a primary partner to regional commercial supply chain leads to understand regional demand planning trends, market access changes, promotional campaigns, and product lifecycle events.
• Ensure demand signals from regional planning teams are accurately reflected and integrated into the end-to-end supply plans.
• Facilitate regular communication and alignment sessions with regional leads to validate assumptions, reconcile forecast discrepancies, and adjust supply plans accordingly.
• Develop, maintain, and execute detailed commercial supply plans that reflect the latest demand insights and manufacturing capacities.
• Utilize SAP ERP and Kinaxis RapidResponse to build and monitor supply plans, adapting quickly to changes in demand or supply constraints.
• Work closely with internal and external manufacturing sites to confirm production schedules support demand trends and commercial priorities.
• Collaborate with regional supply leads to optimize inventory positions, balancing customer service levels with cost efficiency.
• Support supply allocation decisions during constrained supply scenarios by leveraging insights from demand trends.
• Partner with Commercial Operations, Quality, Manufacturing, and Finance teams to ensure supply plans support overall business objectives.
• Monitor and report key supply planning metrics including supply plan adherence, inventory levels, and service performance.

Associate Director, Supply Chain

• Support biostatistical analysis and reporting, document review and data inclusion for NDA submissions of assigned studies
• Collaborate with cross-functional partners to meet clinical development project deliverables and timelines
• Provide statistical consultation on clinical development plans, clinical trial design and clinical study endpoints
• Calculate sample size, author statistical analysis plans and provide biostatistical input into clinical development documentation, scientific publications and presentations, and regulatory filings
• Contribute to short- and long-range Biostatistics strategies, plans and infrastructure development that transcend multiple areas and teams across Biostatistics