Global Clinical Study Lead

BeOne Medicines Ltd.; San Mateo (CA); On-site; USD 150,000 - 190,000; Full time

Job summary

BeOne Medicines Ltd. is seeking a seasoned Clinical Study Project Manager to lead global study delivery from feasibility through closeout, coordinating cross-functional teams and external partners to ensure timely, compliant outcomes.

You will drive study planning, timelines, budgets, risk management, site activation, and regulatory submissions, while mentoring junior staff and partnering with data management, medical writing, and global supplies to optimize quality.

Qualifications

• 7+ years of progressive experience in clinical research within biotech, pharma or CRO
• Proven project management experience in global clinical studies (oncology preferred)
• Advanced knowledge of clinical operations methodologies
• Ability to independently lead global clinical studies
• Bachelor’s degree in a scientific or healthcare discipline; higher degree preferred

Responsibilities

• Lead planning and management from feasibility through closeout
• Generate and maintain high-quality study timelines and track progress
• Oversee trial feasibility, site selection, startup, and activation
• Ensure study plans and TMF are created, updated, and followed
• Monitor compliance with ICH/GCP and quality metrics
• Coordinate with CST, external vendors, data management, and medical writing
• Manage study budgets and vendor relationships

Skills

Cross-functional leadership

Project management

Team mentorship

Education

Bachelor’s Degree in a scientific or healthcare discipline

Advanced degree preferred

Tools

MS Office

Project Planning Applications

Clinical Trial Management Systems

Job description

BeOne Medicines Ltd. is seeking a seasoned Clinical Study Project Manager to lead global study delivery from feasibility through closeout, coordinating cross-functional teams and external partners to ensure timely, compliant outcomes.

You will drive study planning, timelines, budgets, risk management, site activation, and regulatory submissions, while mentoring junior staff and partnering with data management, medical writing, and global supplies to optimize quality.