Teams at Summit Therapeutics, Inc.

Leads pharmacovigilance and medical safety activities for investigational and marketed oncology products. Responsibilities include reviewing individual case safety reports, evaluating adverse events and signals, supporting expedited reporting and unblinding, preparing aggregate safety documents, maintaining reference safety information, coordinating with safety committees and vendors, ensuring regulatory inspection readiness, improving medical safety processes, and mentoring medical safety reviewers.

Leads U.S. regional marketing strategy and commercialization for an oncology biopharmaceutical portfolio. Builds and manages a regional marketing organization, establishes customer and thought-leader engagement strategies, integrates congress and speaker programs, synthesizes market insights, and partners across Marketing, Sales, Medical Affairs, Market Access, Legal, and Compliance. Ensures compliant execution, organizational development, strategic alignment, and effective translation of national brand strategies into regional initiatives.

Leads clinical quality assurance activities across clinical and preclinical programs. Responsibilities include managing clinical site and vendor audits, overseeing quality plans, CAPAs, investigations, inspection readiness, regulatory compliance, vendor issues, and internal audits. The role advises cross-functional teams on GCP, GLP, pharmacovigilance, and global health authority requirements while supporting continuous process improvement and quality risk management.