Incyte

Global Head of R&D & Clinical Development Sourcing

Incyte$150K — $200K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • 10+ years of experience in procurement or sourcing within R&D or clinical services
  • Strong leadership and team management experience
  • Proven ability to influence and collaborate with senior stakeholders
  • Expertise in developing and executing sourcing strategies
  • Comprehensive understanding of clinical development processes and vendor management

Responsibilities

  • Develop and implement multi-year sourcing strategies for R&D and clinical development
  • Act as the primary procurement liaison to R&D and clinical operations teams
  • Drive consensus on sourcing strategies and supplier selections among senior leaders
  • Execute competitive sourcing initiatives including RFPs and contract negotiations
  • Manage supplier performance, governance, and risk assessments
  • Lead and mentor a high-performing procurement team for clinical and R&D categories
  • Enhance sourcing processes for operational excellence and compliance

Benefits

  • Opportunity to lead a strategic and impactful procurement function
  • Collaborative work environment with cross-functional teams
  • Potential for professional growth and leadership development
  • Involvement in cutting-edge R&D processes and innovations
  • Work at an organization committed to speed, quality, and scientific excellence
Full Job Description
Position Summary
The Senior Director, R&D & Clinical Development Sourcing is a strategic leadership role responsible for developing, executing, and optimizing sourcing strategies across all R&D, Clinical Development, and Scientific Services categories. This leader partners closely with Clinical Operations, R&D Leadership, Development Operations, Biometrics, Regulatory, Quality, and Finance to ensure the organization secures best in class CROs, service providers, technology platforms, and scientific suppliers that enable speed, quality, and innovation in the drug development lifecycle.
This role oversees a team of category leads and sourcing managers supporting the end to end value chain for preclinical research, clinical operations, biometrics, scientific services, and external development partnerships. The Senior Director will be responsible for driving strategic supplier management, ensuring operational excellence, enabling cross functional alignment, and delivering measurable value to the organization through cost optimization, risk mitigation, and enhanced performance.

Key Responsibilities
Strategic Leadership & Business Partnership
• Develop a multi year R&D and Clinical Development sourcing strategy aligned with therapeutic, pipeline, and corporate objectives.
• Serve as lead procurement partner to R&D, Clinical Operations, and Development leadership teams.
• Influence senior stakeholders and build consensus around sourcing strategies, supplier selection, and operational models.
• Represent Procurement in governance forums for study planning, vendor oversight, budget management, and external partnerships.
Category Strategy & Value Delivery
• Lead category strategies across CROs, laboratories, bioanalytical services, scientific services, eCOA/eClinical platforms, biometrics, and functional service provider (FSP) models.
• Drive competitive sourcing events, RFPs, master service agreements, and provide input to study level contracting, when necessary.
• Identify and execute cost avoidance, cost savings, operational efficiencies, and value creation initiatives.
• Ensure sourcing strategies consider quality, compliance, capacity, innovation, and risk.
Supplier Relationship Management (SRM)
• Establish and oversee strategic supplier governance across key CROs, labs, and technology providers.
• Partner with QA, Clinical Operations, and Development leadership to manage performance, risk, audits, KPIs, and escalations.
• Develop long term partnerships that support speed, quality, and scientific excellence.
Team Leadership & Development
• Build, lead, and mentor a high performing procurement team that supports clinical and R&D categories.
• Set clear goals, ensure accountability, and champion professional development.
• Embed a culture of collaboration, continuous improvement, and partnership across the team.
Operational Excellence & Process Improvement
• Strengthen sourcing processes related to vendor selection, study startup timelines, bid defenses, governance, and ongoing operational performance.
• Ensure consistent compliance with procurement policies, legal, quality, and regulatory requirements.
• Collaborate with Finance and FP&A to support budget planning, accruals, and necessary forecasting from vendors.
Risk Management & Compliance
• Assess and mitigate vendor, operational, regulatory, and geopolitical risks associated with external R&D/Clinical suppliers.
• Ensure appropriate due diligence, robust contracting, and governance frameworks.

Disclaimer: The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications. Management reserves the right to change or modify such duties as required.

About Incyte

Incyte is a biopharmaceutical company focused on the discovery, development, and commercialization of proprietary therapeutics. The company was founded in 1991 and is headquartered in Wilmington, Delaware. Incyte's main focus is on oncology, inflammation, and autoimmunity. The company's flagship product, Jakafi, is a JAK1/JAK2 inhibitor used to treat myelofibrosis and polycythemia vera. Incyte has a number of other products in development, including itacitinib, a JAK1 inhibitor for the treatment of graft-versus-host disease, and pemigatinib, a FGFR inhibitor for the treatment of cholangiocarcinoma.
Learn more about Incyte
Size
2,094 employees
Market Cap
$17.6 billion
Industry
Net Income
-$295.7 million
Founded
1991
5 Year Trend
+22%
Revenue
$2.6 billion
NASDAQ

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