Teams at Summit Therapeutics, Inc.

Manages clinical pharmacology, pharmacokinetic, drug metabolism, and bioanalytical activities across drug development programs. Responsibilities include designing ADME studies, managing bioanalysis vendors, overseeing PK and ADA sample logistics, ensuring GCP compliance and data integrity, coordinating laboratories and chain of custody, and performing noncompartmental analysis and reporting. The role serves as a clinical pharmacology and DMPK subject matter expert on early- and late-stage cross-functional teams.

Lead portfolio and new-indication strategy for oncology, delivering market and competitive intelligence, forecasting/NPV models, market research, TPP alignment, and cross-functional strategic recommendations to inform executive decisions and BD opportunities.

Lead global regulatory strategy for oncology programs from IND/CTA through BLA/MAA and post‑marketing. Provide cross‑functional regulatory leadership, lead due diligence for partnerships, mentor RA staff, drive labeling and risk‑mitigation strategy, liaise with global authorities, and support product launch activities with minimal oversight.