Associate Director, Clinical Operations

Role: Associate Director, Clinical Operations overseeing global oncology phase II/III trials, ensuring study delivery, quality, compliance, and vendor management. Responsibilities: lead operational planning, oversee CROs and vendors, manage budgets, ensure inspection readiness, and foster cross-functional collaboration across clinical functions including Regulatory, Data Management, and Quality. Require 10+ years in clinical trial management, with proven expertise in international oncology studies, GCP/ICH guidelines, and vendor oversight. Preferred skills include strong problem-solving, leadership, negotiation, and deep understanding of drug development stages and regulations. High-value specifics: global phase II/III oncology trials, focus on NSCLC and CRC, oversight of complex, multi-center studies, vendor governance, and regulatory inspection preparedness. Work setup involves international travel (up to 20%), with a focus on operational excellence in a fast-paced environment.