Clinical Trials Lead Nurse Coordinator

Washington University in St. Louis; Ann Arbor (MI); On-site; USD 65,000 - 110,000; Full time

Benefits offered by this job

Up to 22 days of vacation, holidays, &

Competitive health insurance packages

Metro transit U-Pass for eligible

401(k) Retirement Savings Plan

Job summary

Washington University in St. Louis is seeking a Research Nurse Coordinator to lead enrollment and ensure adherence to study procedures. You will coordinate regulatory submissions, supervise staff, and manage clinical trial activities with a focus on data integrity and participant safety.

The role involves direct patient care, protocol compliance, and collaboration with multidisciplinary teams to support high-quality research outputs.

Qualifications

• Associate Degree in Nursing or Diploma in Registered Nursing required.
• Basic Life Support certification required; other licenses preferred.
• 2 years in Research and Nursing experience referenced in posting.

Responsibilities

• Lead coordination of enrollment and study procedures per protocol.
• Manage IRB submissions, budgets, and regulatory ensure compliance.
• Provide direct patient care and data collection for the study.
• Train/supervise staff and coordinate specimen handling and reporting.
• Prepare and submit reportable event reports to sponsors and IRBs.

Skills

Active Listening

Clinical Research Coordination

Clinical Research Management

Clinical Research Methods

Clinical Research Operations

Clinical Techniques

Database Management

Detail-Oriented

Electronic Health Records (EHR)

Nursing Fundamentals

Oral Communications

Patient Recruitment

Reporting Tools

Spreadsheet Software

Statistical Analysis Software (SAS)

Team Collaboration

Education

Associate Degree In Nursing Or Diploma In Registered Nursing

Tools

SAS

EHR Systems

Job description

Washington University in St. Louis is seeking a Research Nurse Coordinator to lead enrollment and ensure adherence to study procedures. You will coordinate regulatory submissions, supervise staff, and manage clinical trial activities with a focus on data integrity and participant safety.

The role involves direct patient care, protocol compliance, and collaboration with multidisciplinary teams to support high-quality research outputs.