Director, Clinical Operations

Role: The Director of Clinical Operations for Oncology leads global execution of Phase I-IV oncology trials, ensuring high-quality, timely, and compliant study delivery. Responsibilities include overseeing a large team, developing operational strategies, managing budgets, and representing Clinical Operations in cross-functional and strategic teams. The role involves vendor oversight, risk management, process optimization, and contributing to development plans and organizational initiatives. Requirements: BA/BS/RN with 12+ years or advanced degree with 10+ years, specific experience in oncology clinical trials, proven leadership in complex programs, CRO/vendor management skills, and extensive knowledge of regulatory standards (FDA, EMA, ICH, GCP). Preferred qualifications include experience managing cross-functional teams, strategic planning, and change management. High-value details: focus on registration-stage oncology trials, expertise in endpoints and trial design specific to oncology, and experience with global clinical development. The position demands strong stakeholder engagement, leadership, and communication skills, with occasional national/international travel. Work setup: not explicitly specified, but implies a leadership role with potential travel.