Remote Clinical Trials Manager

Washington University in St. Louis; United States; Remote; USD 75,000 - 129,000; Full time

Benefits offered by this job

Up to 22 days of vacation

10 holidays and sick time

Health insurance

Metro transit U-Pass

Tuition assistance (401(k)/403(b)

Job summary

Washington University in St. Louis is seeking a senior supervisor to oversee Functional Research Groups, train coordinators, manage budgets, and ensure high-quality data in clinical trials. The role includes staff leadership, regular evaluations, and collaboration with oncologists to guide study progress.

The position emphasizes regulatory compliance, data integrity, and strategic planning for current and upcoming studies within institutional and industry-sponsored trials.

Qualifications

• Bachelor’s degree or combination of education and/or experience may substitute for minimum education.
• No specific certification/professional license is required for this position.
• Clinical Research experience (1 Year)
• A driver’s license is not required for this position.

Responsibilities

• Leads Functional Research Groups; hires and staffs; orients and trains staff; plans budgets and staffing; conducts performance evaluations.
• Oversees daily activities of Senior Research Coordinators; ensures protocol compliance and data quality; monitors data accuracy.
• Supports QA processes and regulatory adherence through the QASMC committee; monitors study progress and coordination with oncologist; plans upcoming studies.
• Performs other duties as assigned.

Skills

Clinical project management

Clinical systems

Clinical trials administration

Deadline management

Interpersonal relationships

Leadership

Microsoft Excel

Microsoft Word

Oral communications

Prioritization

SQL databases

Stress management

Written communication

Education

Bachelor’s degree

Job description

Washington University in St. Louis is seeking a senior supervisor to oversee Functional Research Groups, train coordinators, manage budgets, and ensure high-quality data in clinical trials. The role includes staff leadership, regular evaluations, and collaboration with oncologists to guide study progress.

The position emphasizes regulatory compliance, data integrity, and strategic planning for current and upcoming studies within institutional and industry-sponsored trials.