Associate Director, Clinical Operations Program Lead

Role: Associate Director, Clinical Operations Program Lead in Oncology, responsible for developing and executing operational strategies for clinical programs, ensuring timely, high-quality study delivery within budget. Responsibilities include representing Clinical Operations at the Global Program Team, collaborating with cross-functional teams, overseeing vendor performance, managing budgets, and contributing to process improvements. Qualifications: Bachelor's in Life Sciences or related field; 10+ years in pharma/clinical research, with 7+ years in study/project management, especially early or later-phase global oncology trials; expertise in regulatory compliance (e.g., GCP, CFR, CTD); strong leadership, communication, and risk management skills; experience with cross-functional initiatives and inspection readiness. Preferred: Advanced degree, experience across multiple therapeutic areas, and fluency in business English. HighValue: Oncology clinical development, global Phase 2 or later studies, vendor oversight, regulatory compliance, program management, and strategic leadership. WorkSetup: Remote Massachusetts; no specific travel noted.