Senior Global Clinical Study Coordinator

BeOne Medicines USA; United States; On-site; USD 65,000 - 95,000; Full time

Job summary

BeOne Medicines USA is seeking an experienced clinical research professional to support global study delivery. You will align study goals with clinical operations and assist in vendor management, budgeting, and deliverable tracking.

The role requires collaboration with regional teams, knowledge of ICH-GCP, and strong MS Office and project-management skills to ensure high quality, timely execution of studies in the biotech/pharma space.

Qualifications

• 3+ years of clinical research experience in Biotech/Pharma/CRO.
• Bachelor or higher degree in scientific or healthcare discipline.
• Knowledge of clinical operations methodologies and regulatory requirements (ICH-GCP).
• Proficiency in MS Office Suite (Excel, PowerPoint) and project management tools.

Responsibilities

• Support the Global Clinical Study Manager with study planning and execution.
• Coordinate cross-functional CST meetings and document sharing.
• Assist with TMF creation and study drug forecasts.
• Monitor study deliverables and prepare management metrics.

Skills

Cross-functional collaboration

Regulatory knowledge

Leadership support

Education

Bachelor or higher degree in scientific or healthcare discipline

Tools

MS Office Suite

Excel

PowerPoint

Project

Job description

BeOne Medicines USA is seeking an experienced clinical research professional to support global study delivery. You will align study goals with clinical operations and assist in vendor management, budgeting, and deliverable tracking.

The role requires collaboration with regional teams, knowledge of ICH-GCP, and strong MS Office and project-management skills to ensure high quality, timely execution of studies in the biotech/pharma space.