Global Oncology Clinical Study Lead

BeiGene Ltd.; United States; Remote; USD 119,000 - 159,000; Full time

Benefits offered by this job

Medical benefits

Dental benefits

Vision insurance

401(k)

Paid time off

Wellness program

Job summary

BeOne Medicines Ltd. in the United States is seeking an experienced Clinical Study Manager to lead global oncology studies from feasibility through closeout.

You will drive cross-functional study teams, manage external vendors, and coordinate with regulatory and medical writing groups to deliver high-quality data. The ideal candidate has 5+ years in clinical research, pivotal oncology study experience, and strong project leadership.

Qualifications

• 5+ years of progressive experience in clinical research
• Experience in global oncology studies, preferably pivotal studies
• Pivotal study management experience required
• Ability to independently lead global clinical studies and cross-functional teams
• Experience managing external vendors and CROs

Responsibilities

• Leads the global cross-functional study team and external vendors
• Plans and manages studies from feasibility through closeout
• Ensures timely study documents for regulatory submissions
• Oversees trial feasibility, site activation, and data management
• Maintains study budgets and resource planning
• Ensures inspection readiness and quality metrics
• Collaborates with CST members and other stakeholders

Skills

Global clinical studies

Project management

Oncology experience

Stakeholder collaboration

Regulatory familiarity

Education

Bachelor's degree in science/healthcare

Higher degree preferred

Tools

MS Office

Project Planning Applications

Clinical Trial Management Systems

Job description

BeOne Medicines Ltd. in the United States is seeking an experienced Clinical Study Manager to lead global oncology studies from feasibility through closeout.

You will drive cross-functional study teams, manage external vendors, and coordinate with regulatory and medical writing groups to deliver high-quality data. The ideal candidate has 5+ years in clinical research, pivotal oncology study experience, and strong project leadership.