Global Clinical Study Coordinator

BeiGene Ltd.; United States; Remote; USD 73,000 - 98,000; Full time

Job summary

BeOne Medicines Ltd. in the United States seeks a Clinical Operations Associate to support the Global Clinical Study Manager in delivering global studies with quality, timelines, and budget adherence.

You will coordinate CST meetings, manage study information in eTMF/CTMS/SharePoint, ensure system access, assist with study plans, TMF QC, and data-related activities while collaborating with cross-functional teams and vendors.

Qualifications

• Bachelor or higher degree in scientific or healthcare field; higher degree preferred.
• 1+ year of clinical research experience in biotech, pharma or CRO.
• Knowledge of clinical operations and regulatory guidelines.
• Proficiency with MS Office and project management tools.

Responsibilities

• Coordinate CST meetings and cross-functional collaboration.
• Set up and maintain study info in systems (eTMF, CTMS, SharePoint).
• Manage access and user accounts across the study lifecycle.
• Assist with study plans, TMF QC, and data handling activities.
• Support study drug forecasts and supply activities.
• Prepare metrics and communications for the study team.

Skills

MS Office

Clinical operations knowledge

Clinical research experience

Travel willing

Education

Bachelor or higher degree in a scientific or healthcare discipline

Tools

SharePoint

CTMS

eTMF

MS Office

Job description

BeOne Medicines Ltd. in the United States seeks a Clinical Operations Associate to support the Global Clinical Study Manager in delivering global studies with quality, timelines, and budget adherence.

You will coordinate CST meetings, manage study information in eTMF/CTMS/SharePoint, ensure system access, assist with study plans, TMF QC, and data-related activities while collaborating with cross-functional teams and vendors.