Director, Sourcing & Procurement

Summit Therapeutics, Inc.; United States; On-site; USD 190,000 - 237,000; Full time

Job summary

Summit Therapeutics, Inc. is seeking a Director, Sourcing & Procurement – R&D Clinical Operations to partner with Clinical Ops, R&D, and Finance. You will lead strategic sourcing, supplier selection, and governance for CROs, central labs, imaging vendors, and other eClinical providers.

This role drives cost efficiency and process improvement across global clinical studies. You will negotiate terms, manage budgets, and build cross-functional governance models to optimize study

Qualifications

• Minimum BA/BS degree or relevant graduate degree preferred.
• 10+ years experience in Procurement, Vendor Management or Finance in pharma/CRO settings.
• Strong knowledge of GCP/ICH guidelines for clinical operations.
• Experience with CROs, central labs, imaging, and supply vendors is a plus.
• Excellent negotiation, governance, and contract management capabilities.

Responsibilities

• Lead strategic sourcing and commercial guidance across study planning, startup, execution, and closeout.
• Develop supplier strategies for Clinical Operations and related R&D categories.
• Direct end-to-end CRO/central labs/imaging/eCOA/vendor sourcing activities.
• Translate study requirements into effective procurement plans and vendor solutions.
• Provide market intelligence, bid analysis, and vendor recommendations for budgeting.
• Negotiate MSAs, SOWs, and pricing with Legal and Finance input.
• Oversee budgets, change orders, and invoices to identify cost savings.
• Establish vendor governance with scorecards, KPIs, and risk mitigation.
• Identify supplier risks and ensure study timelines and continuity.

Skills

Procurement

Contract management

Vendor management

GCP/ICH

MS Office

Cross-functional

Attention to detail

Analytical thinking

Problem solving

Independent work

Education

BA/BS degree or higher

Tools

Ariba

Coupa

Veeva Vault

Job description

About Summit

Summit Therapeutics Inc. is a biopharmaceutical oncology company with a mission focused on improving quality of life, increasing potential duration of life, and resolving serious unmet medical needs. At Summit, we believe in building a team of world class professionals who are passionate about this mission, and it is our people who drive this mission to reality. Summit’s core values include integrity, passion for excellence, purposeful urgency, collaboration, and our commitment to people. Our employees are truly the heart and soul of our culture, and they are invaluable in shaping our journey toward excellence.

About Summit

Summit Therapeutics Inc. is a biopharmaceutical oncology company with a mission focused on improving quality of life, increasing potential duration of life, and resolving serious unmet medical needs. At Summit, we believe in building a team of world class professionals who are passionate about this mission, and it is our people who drive this mission to reality. Summit’s core values include integrity, passion for excellence, purposeful urgency, collaboration, and our commitment to people. Our employees are truly the heart and soul of our culture, and they are invaluable in shaping our journey toward excellence.

Summit’s Team Is Inspired To Touch And Help Change Lives Through Summit’s Clinical Studies In The Field Of Oncology. Summit Has Multiple Global Phase 3 Clinical Studies, Including

Non-small Cell Lung Cancer (NSCLC)

• HARMONi: Phase 3 clinical study which was intended to evaluate ivonescimab combined with chemotherapy compared to placebo plus chemotherapy in patients with EGFR-mutated, locally advanced or metastatic non-squamous NSCLC who were previously treated with a 3rd generation EGFR TKI.
• HARMONi-3: Phase 3 clinical study which is intended to evaluate ivonescimab combined with chemotherapy compared to pembrolizumab combined with chemotherapy in patients with first-line metastatic NSCLC.
• HARMONi-7: Phase 3 clinical study which is intended to evaluate ivonescimab monotherapy compared to pembrolizumab monotherapy in patients with first-line metastatic NSCLC.

Colorectal Cancer (CRC)

• HARMONi-GI3: Phase 3 clinical study intended to evaluate ivonescimab in combination with chemotherapy compared with bevacizumab plus chemotherapy.

Ivonescimab is an investigational therapy not presently approved by any regulatory authority other than China’s National Medical Products Administration (NMPA). Summit is headquartered in Miami, Florida, and has additional offices in California, New Jersey, the UK, and Ireland.

Overview Of Role

The Director, Sourcing & Procurement – R&D Clinical Operations and Supplies will serve as business partner supporting sourcing strategy, contracting, and governance activities across Summit’s Clinical Operations organization and global clinical trial portfolio. This individual will report to the Head of Procurement. The role is responsible for supporting the selection, contracting, and oversight of key clinical service providers, including CROs, central laboratories, imaging vendors, eCOA and other eClinical technology providers, patient recruitment and retention suppliers, investigator payment providers, specialty service vendors, and clinical trial supply partners. The position may also support clinical supply and logistics-related procurement activities, helping ensure the timely and cost-effective delivery of materials and services required to execute global clinical studies. The breadth of this role provides significant exposure across the end-to-end clinical development lifecycle and the opportunity to influence sourcing strategy, supplier performance, and operational execution across the clinical portfolio.

Working closely with Clinical Operations, R&D, Clinical Supply Chain, Finance, Legal, and other cross-functional stakeholders, this individual will help drive vendor strategy, optimize study-related spending, improve sourcing and contracting processes, mitigate supplier risks, and establish effective governance models with critical suppliers. As Summit continues to grow and expand its clinical development portfolio, this role will have opportunities to support additional R&D and Commercial procurement categories and contribute to broader procurement transformation, process improvement, and vendor management initiatives across the organization.

Role And Responsibilities

• Serve as a lead/procurement business partner to Clinical Operations, providing strategic sourcing and commercial guidance throughout study planning, startup, execution, and closeout.
• Develop and execute category and supplier strategies across Clinical Operations, Clinical Trial Supplies, and related R&D categories, balancing quality, compliance, service continuity, speed, and total cost.
• Lead end-to-end competitive sourcing activities across CROs, central laboratories, imaging, eCOA and eClinical technology, IRT/RTSM, patient recruitment and retention, investigator payments, specialty clinical services, logistics, and clinical trial supply vendors.
• Partner with Clinical Operations, R&D, and Clinical Supply Chain to translate study requirements, timelines, enrollment assumptions, and supply needs into effective sourcing plans and fit-for-purpose vendor solutions.
• Provide commercial insights, market intelligence, benchmarking, bid analysis, and supplier recommendations to support study feasibility, budgeting, vendor selection, and executive decision-making.
• Lead negotiation and review of MSAs, SOWs, work orders, rate cards, pricing models, service levels, and other commercial terms in collaboration with Legal, Finance, and business stakeholders.
• Support financial oversight of outsourced clinical services by reviewing study budgets, change orders, scope modifications, forecasts, and supplier invoices to improve cost transparency, challenge unsupported charges, and identify savings or cost-avoidance opportunities.
• Establish and facilitate vendor governance for strategic clinical and supply partners, including business reviews, performance scorecards, KPIs and SLAs, issue escalation, risk mitigation, and continuous improvement plans.
• Proactively identify and help resolve supplier risks affecting study execution, including performance concerns, capacity constraints, timeline impacts, supply continuity, logistics dependencies, quality events, and contract compliance.
• Contribute as a procurement generalist to broader enterprise priorities, including process standardization, sourcing tools, spend analytics, supplier rationalization, AI and automation projects, and other procurement transformation initiatives.

Experience, Education And Specialized Knowledge And Skills

• Minimum BA/BS degree or relevant graduate degree preferred
• Minimum of 10+ years of experience in a Procurement/Vendor Management or Finance environment in a pharmaceutical, CRO/ biotech company or worked in a clinical R&D operations setting with a CRO/Sponsor company
• Good understanding of the drug development R&D process is important
• In-depth understanding of clinical trial-related execution of large global studies, including CROs, central labs, imaging, drug supply, CMC vendors, and ancillary suppliers. Oncology experience preferred.
• Strong knowledge of GCP, ICH, and regulatory expectations governing outsourced clinical activities
• Demonstrated ability to multi-task, prioritize, and independently solve problems in a rapidly changing environment
• Proficient user of standard MS Office suite (e.g., Word, Excel), experience using electronic document management systems (e.g. Veeva Vault, etc.), and document review tools desirable
• Strong computer and database skills and experience with procurement or contract management systems (e.g. Ariba, Coupa, etc.)
• Attention to detail, accuracy and confidentiality with clear and concise oral and written communication skills
• Excellent organizational skills
• Critical thinking, problem solving, ability to work independently
• Demonstrated ability to collaborate cross-functionally, manage competing priorities, and operate in a fast-paced, high growth organization

This is the pay for this position

Pay Transparency

$190,000 - $237,000 USD

Actual compensation packages are based on several factors that are unique to each candidate, including but not limited to skill set, depth of experience, certifications, and specific work location. This may be different in other locations due to differences in the cost of labor. The total compensation package for this position may also include bonus, stock, benefits and/or other applicable variable compensation.

Summit Therapeutics Inc. is an Equal Opportunity Employer and takes pride in creating and maintaining diverse environment. We do not discriminate in recruitment, hiring, training or promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status.