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Director, GCO Program Lead (GCPL)

BeOne Medicines
August 20, 2026
Full-time
Remote friendly (United States)
Worldwide
Clinical Research and Development
Role: GCO Program Lead responsible for strategic operational planning and clinical performance oversight of designated cancer programs, leveraging deep therapeutic expertise. Responsibilities: lead global cross-functional teams including gCSMs, drive program strategy, resource and budget management, oversee study execution, and ensure quality and regulatory compliance; mentor and develop team members; collaborate with stakeholders to optimize clinical operations; act as GCO representative for assigned programs; lead risk management and process improvements. Requirements: Bachelor's or higher in a scientific or healthcare discipline; 10+ years' experience in clinical trials, including program and people management; strong knowledge of ICH/GCP guidelines, clinical documentation, data, and risk management. Preferred: experience in multi-region trials, project management, and cross-functional collaboration. High-Value: Oncology (cancer), global program management, clinical operations, risk and issue management, stakeholder engagement, and leadership in a fast-paced, international environment. Work setup: travel may be required as per business needs.