Associate Director, Clinical Operations

Summit Therapeutics, Inc.

Role Associate Director, Clinical Operations leading global oncology Phase 2/3 trials, including NSCLC and CRC indications, with a focus on operational execution and vendor management. Responsibilities oversee clinical trial planning ensuring compliance with GCP/ICH manage CROs and external vendors mitigate operational risks control budgets maintain inspection readiness foster cross-functional collaboration across Regulatory, Clinical Science, Data Management, and Quality teams Lead the development and approval of study plans manage TMF quality drive process improvements Qualifications Bachelor's degree in life sciences or related field; 10+ years of experience managing international oncology clinical trials, with strong leadership, regulatory, and operational expertise. Preferred deep knowledge of drug development, GCP/ICH, and complex global study execution. High-Value Oncology (NSCLC, CRC), Phase 2/3, international, vendor oversight, inspection readiness, cross-functional leadership. Work Setup not specified; travel up to 20%. #J-18808-Ljbffr

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Vacancy posted 5 days ago

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