Director, GCO Clinical Program Lead (GCPL)

Role: GCO Program Lead responsible for strategic operational planning and clinical performance of designated oncology programs within BeOne’s integrated development platform. Responsibilities: lead and develop global Clinical Study Managers, oversee study delivery and budget, act as GCO representative for program strategy, mentor team, and collaborate cross-functionally to ensure high-quality trial execution aligned with regulatory standards and GxP. Manage external partner studies via the Clinical SuperHighway, provide operational insights to shape program strategy, and serve as escalation point for study issues. Requirements: Bachelor’s or higher in a scientific or healthcare field, 10+ years in clinical trials with experience in global program and people management, deep knowledge of ICH/GCP guidelines, and proficiency with CTMS and project management tools. Preferred: experience in oncology (cancer-focused), multi-region trials, and leadership in fast-paced environments. High-Value: Oncology, global multi-region trials, leadership in clinical operations, external partnership management, and strategic program oversight. WorkSetup: international role with up to 20% travel.