Teams at Summit Therapeutics, Inc.

Leads global clinical trial site agreement strategy, budget development, contract and budget negotiations, payment forecasting, and site activation activities. Partners with Legal, Finance, Clinical Operations, CROs, FSPs, and research sites to ensure compliant, cost-effective agreements and timely study execution. Oversees vendors, resolves contract and payment issues, develops outsourcing strategies, monitors performance, and improves departmental processes across large, multi-site clinical trials.

Supports and optimizes corporate G&A applications for Finance, HR, and Legal, including NetSuite, Coupa, Agiloft, HRIS, and CLM systems. Translates business needs into technical requirements, manages application health, builds reports and dashboards, supports SOX ITGC controls and audits, coordinates testing and implementations, and develops training and documentation.

Provides GMP quality oversight across biologics development and manufacturing, including CMOs, CTLs, process validation, technology transfer, change controls, comparability, quality systems, inspections, investigations, CAPA, risk management, and CMC regulatory submissions. Partners with MSAT and Technical Operations, leads quality improvement initiatives, manages product quality reviews and metrics, and ensures compliance with global GMP requirements throughout the product lifecycle.