Associate Director, Clinical Operations

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, and foster cross-functional collaboration across Regulatory, Clinical Science, Data Management, and Quality teams. Lead the development and approval of study plans, manage TMF quality, and 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%.