Senior Clinical Trials Nurse Coordinator

Washington University in St. Louis

Ann Arbor (MI)

On-site

USD 65,000 - 110,000

Full time

14 days+

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Benefits offered by this job

Up to 22 days vacation
Competitive health insurance packages
Metro transit U-Pass
Tuition assistance for you and family

Job summary

Washington University in St. Louis in Saint Louis, MO is seeking a capable Clinical Research Nurse Coordinator to lead enrollment and oversee multiple clinical trials.

You will coordinate start-up activities, ensure protocol adherence, and supervise staff while maintaining regulatory compliance and data integrity. The role requires direct patient care, data collection, and collaboration with PI and sponsor teams.

Qualifications

  • BLS certification is required (Basic Life Support).
  • Clinical Research Certification is preferred.

Responsibilities

  • Coordinate enrollment of study subjects and supervise staff.
  • Manage IRB submissions and regulatory requirements.
  • Provide direct patient care, data collection and physician support.
  • Identify, screen and enroll study subjects with the research team.
  • Ensure protocol adherence and data handling per study plan.
  • May train staff on study procedures and adverse events.
  • Oversee study medications and investigational products as appropriate.
  • Prepare and submit reportable event reports to sponsors and IRBs.

Skills

Direct patient care
Clinical research coordination
Clinical research management
Clinical research methods
Clinical research operations
Clinical techniques
Database management
Detail-oriented
Effective written communication
Electronic Health Records (EHR)
Nursing fundamentals
Oral communications
Patient recruitment
Reporting tools
Spreadsheet software
SAS (Statistical Analysis Software)
Team collaboration

Education

B.S. - Bachelor of Science - Nursing

Job description

Washington University in St. Louis in Saint Louis, MO is seeking a capable Clinical Research Nurse Coordinator to lead enrollment and oversee multiple clinical trials.

You will coordinate start-up activities, ensure protocol adherence, and supervise staff while maintaining regulatory compliance and data integrity. The role requires direct patient care, data collection, and collaboration with PI and sponsor teams.

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