Associate Director, Specialty Laboratory Sourcing, Contracting and Category Management
Gilead Sciences
Summary
The Associate Director, Vendor Outsourcing, focused on Specialty Laboratory Sourcing, Contracting and Category Management serves as the category partner and subject matter expert for Biomarker, Bioanalytical, and Companion Diagnostics across Clinical Development and Research. The role is responsible for developing and executing the category strategy, leading strategic sourcing initiatives, negotiating and executing complex agreements and managing vendor relations to deliver quality, compliance, innovation and value.
Job description
Key Responsibilities
Category Strategy and Portfolio Management
- Develop, maintain, and execute the Specialty Laboratory category strategy for Biomarker, Bioanalytical, and Companion Diagnostic laboratory services.
- Lead category reviews, including marketplace analysis, demand and spend assessment, vendor segmentation, capability mapping, benchmarking, and identification of core competencies.
- Manage the portfolio of strategic core and niche laboratories based on scientific capability, quality, capacity, geographic reach, innovation, risk, performance, and total value.
- Develop and manage category-level standards that can be applied across the laboratory portfolio.
- Monitor market practices, technologies, emerging vendors, and internal demand to recommend portfolio changes and fit-for-purpose sourcing approaches.
Stakeholder Management and Scientific Partnership
- Serve as the primary Vendor Outsourcing point of contact for specialty lab services.
- Provide strategic consultation to business stakeholders on vendor strategy and market dynamics.
- Build trusted relationships with Biomarker Operations, Clinical Pharmacology, Kite Translational Medicine, therapeutic-area research scientists, Clinical Operations, and other key partners.
- Translate scientific and business requirements into laboratory sourcing strategies, vendor recommendations, contracting approaches, and implementation plans.
- Influence senior internal stakeholder decisions and external laboratory partners on contractual, commercial, operational, legal, and regulatory matters.
Contracting and Commercial Terms Management
- Lead contract negotiations in partnership with functional leaders and Legal, translating business and scientific requirements into appropriate contractual and commercial terms.
- Manage the development, negotiation, execution, maintenance, and renewal of master laboratory agreements and master service agreements for core and niche laboratories.
- Lead amendments to master agreements, including updates required for new services, capabilities, technologies, legal terms, compliance requirements, or changes to the commercial framework.
- Manage rate cards and related pricing structures; use internal and external benchmarking and market assessments to ensure pricing is at or below fair market value where supported by scope, service level, geography, quality, and technical requirements.
- Negotiate CDx agreements with commercialization terms including milestones and royalty structures with direction from legal.
- Oversee scopes of work, change orders, budgets, and related contracting documents to maintain alignment with the governing master agreement and approved commercial terms.
- Identify and execute category-level cost-containment and cost-avoidance opportunities through benchmarking, negotiation, demand management, rate-card discipline, and portfolio leverage.
- Maintain appropriate contract records and support compliant execution, inspection readiness, and agreement closeout.
- Lead the onboarding of new core and niche laboratories in partnership with Vendor Qualification, Quality, Legal, Compliance, Privacy, Security, Finance, functional stakeholders, and other required groups.
- Collaborate with Vendor Performance and Relationship Management to address performance, capacity, quality, timeline, compliance, and business-continuity risks.
- Support inspection-readiness activities, audit responses, regulatory and contractual compliance, data privacy, and protection of intellectual property.
Problem Solving and Continuous Improvement
- Proactively monitor vendor performance and drive continuous improvement initiatives.
- Recommend innovative or alternative laboratory sourcing solutions through effective stakeholder management and structured evaluation of vendor capabilities.
- Use benchmarking analytics and industry best practices to improve sourcing, contracting, onboarding, governance, vendor performance, and cycle times.
- Support new data sources and technologies that enable efficient clinical-trial and research execution.
Capabilities and Requirements
- Demonstrated experience leading a specialty laboratory category, laboratory vendor portfolio, strategic sourcing area, or related function in biopharmaceutical, biotechnology, clinical research, diagnostic, or laboratory services.
- Knowledge of Biomarker, Bioanalytical, Companion Diagnostic, translational medicine, and/or related specialty laboratory services.
- Strong category-management capabilities, including category strategy, marketplace analysis, vendor segmentation, capability mapping, category reviews, benchmarking, governance, and value delivery.
- Strong stakeholder-management and influencing skills across scientific, clinical, operational, legal, financial, quality, compliance, regulatory, and vendor organizations.
- Demonstrated contracting expertise, including negotiation and maintenance of master laboratory agreements or master service agreements, amendments, scopes of work, change orders, budgets, and rate cards.
- Experience onboarding new vendors and coordinating qualification, contracting, operational setup, and governance.
- Financial and commercial acumen, including fair-market-value assessment, cost-driver analysis, benchmarking, rate negotiation, cost avoidance, and spend optimization.
- Ability to solve complex problems, manage multiple priorities, communicate recommendations clearly, and maintain momentum in a matrixed global environment.
- Experience leading experienced professionals, cross-functional teams, and/or direct reports, as applicable.
Education and Preferred Credentials
- Bachelor's degree in a scientific, medical, business, finance, supply-chain, or related discipline w/10+ years of experience
- Advanced degree in a scientific, medical, business, finance, supply-chain, or related discipline is preferred
- MA/MS w/8+ years of experience
- PhD/PharmD/JD w/5+ years of experience
- Professional certification in supply management, procurement, contracting, project management, or a related discipline is preferred.
- Travel may be required.
Requirements
- Demonstrated experience leading a specialty laboratory category, laboratory vendor portfolio, strategic sourcing area, or related function in biopharmaceutical, biotechnology, clinical research, diagnostic, or laboratory services.
- Knowledge of Biomarker, Bioanalytical, Companion Diagnostic, translational medicine, and/or related specialty laboratory services.
- Strong category-management capabilities, including category strategy, marketplace analysis, vendor segmentation, capability mapping, category reviews, benchmarking, governance, and value delivery.
- Strong stakeholder-management and influencing skills across scientific, clinical, operational, legal, financial, quality, compliance, regulatory, and vendor organizations.
- Demonstrated contracting expertise, including negotiation and maintenance of master laboratory agreements or master service agreements, amendments, scopes of work, change orders, budgets, and rate cards.
- Experience onboarding new vendors and coordinating qualification, contracting, operational setup, and governance.
- Financial and commercial acumen, including fair-market-value assessment, cost-driver analysis, benchmarking, rate negotiation, cost avoidance, and spend optimization.
- Ability to solve complex problems, manage multiple priorities, communicate recommendations clearly, and maintain momentum in a matrixed global environment.
- Experience leading experienced professionals, cross-functional teams, and/or direct reports, as applicable.
- Bachelor's degree in a scientific, medical, business, finance, supply-chain, or related discipline w/10+ years of experience
- Advanced degree in a scientific, medical, business, finance, supply-chain, or related discipline is preferred
- MA/MS w/8+ years of experience
- PhD/PharmD/JD w/5+ years of experience
- Professional certification in supply management, procurement, contracting, project management, or a related discipline is preferred.
Benefits
- Medical Insurance
- Dental Insurance
- Vision Insurance
- Life Insurance
- Paid Time Off
- Annual Bonus
- Stock-Based Long-Term Incentives
Company overview
Gilead Sciences, Inc. is a leading American biopharmaceutical company headquartered in Foster City, California, that specializes in researching, developing, and commercializing innovative medicines for life-threatening diseases. Founded in 1987, Gilead has grown into a global healthcare leader with approximately 17,600 employees worldwide. The company's primary therapeutic focus areas include HIV/AIDS, viral hepatitis (hepatitis B and C), oncology, inflammation, and respiratory diseases. Gilead is renowned for its groundbreaking antiviral therapies, including Sovaldi and Harvoni for hepatitis C, and its comprehensive portfolio of HIV treatments such as Truvada, Atripla, and Biktarvy. The company also developed Veklury (remdesivir) for COVID-19 treatment. Gilead operates as a publicly traded company on the NASDAQ (GILD) and is a component of both the Nasdaq-100 and S&P 100 indices. Through strategic acquisitions like Kite Pharma and Immunomedics, Gilead has expanded into cell therapy and oncology, demonstrating its commitment to advancing medical science and improving patient outcomes globally.