Clinical Research Coordinator Ii - Cardiology

Washington University in St. Louis

St. Louis, Missouri, US
Base: $52,600.00 - $78,900.00 annually; bonus/equi...
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Independent coordination of multiple funded studies
Regulatory compliance with ich-gcp and nih policies
Irb application submission and maintenance
** Washington University in St. Louis is seeking a Clinical Research Coordinator II (CRC II) to manage and coordinate complex clinical research activities within its Cardiovascular Division. The ideal candidate should have a background in clinical research, be detail-oriented, and possess the ability to manage multiple studies effectively while ensuring compliance with regulatory guidelines. **

Job Summary

  • The role serves as a key operational lead and liaison among the PI, study teams, institutional offices, sponsors, and external collaborators.
  • Candidates must independently coordinate day-to-day operations of multiple funded clinical research studies while ensuring regulatory compliance and data integrity.
  • Washington University offers competitive benefits including up to 22 days of vacation, comprehensive health insurance, and tuition coverage for employees and families.

Matching Summary

Match Score: 75

** Washington University in St. Louis is seeking a Clinical Research Coordinator II (CRC II) to manage and coordinate complex clinical research activities within its Cardiovascular Division. The ideal candidate should have a background in clinical research, be detail-oriented, and possess the ability to manage multiple studies effectively while ensuring compliance with regulatory guidelines. **

Salary

Base: $52,600.00 - $78,900.00 annually; Bonus/Equity: Not specified; Benefits: Up to 22 days vacation, health insurance, retirement plan, tuition coverage

Skills & Requirements

Must-have

  • Independent coordination of multiple funded studies
  • Regulatory compliance with ICH-GCP and NIH policies
  • IRB application submission and maintenance
  • Data collection quality control and documentation
  • Study start-up protocol development

Nice-to-have

  • Proactive management of competing priorities
  • Experience with international research projects
  • Assistance with grant proposal preparation
  • Literature review for study planning

Key Requirements

  • Bachelor's degree or equivalent experience
  • 2 years of Clinical Research work experience
  • Basic Life Support certification (with skills assessment)
  • Driver's license not required

Work Rights

Not specified

Tailored Resume

Cover Letter