Clinical Research Coordinator 4

VUMC (Vanderbilt University Medical Center)

Nashville, Tennessee, US
Hybrid
5 years relevant research experience
Socra certified clinical research professional
Irb submission and amendment experience
This pivotal role leads the daily operations of the multi-site DOSE Trial with minimal supervision while ensuring high-quality study conduct and regulatory compliance

Job Summary

  • This pivotal role leads the daily operations of the multi-site DOSE Trial with minimal supervision while ensuring high-quality study conduct and regulatory compliance.
  • The successful candidate will supervise research staff, facilitate steering committee meetings, and maintain protocol adherence across all participating sites.
  • Vanderbilt University Medical Center offers a comprehensive benefits package and fosters an environment where employees are part of something bigger than themselves.

Matching Summary

This pivotal role leads the daily operations of the multi-site DOSE Trial with minimal supervision while ensuring high-quality study conduct and regulatory compliance.

Skills & Requirements

Must-have

  • 5 years relevant research experience
  • SOCRA Certified Clinical Research Professional
  • IRB submission and amendment experience
  • Multi-site trial coordination
  • REDCap database management
  • Staff supervision and training

Nice-to-have

  • Spanish language skills preferred
  • Experience with culturally responsive communication
  • Manuscript and grant writing support
  • Collaborative team culture promotion

Key Requirements

  • Bachelor's Degree or equivalent experience
  • SOCRA Certification required
  • Minimum 5 years research experience
  • Previous IRB experience required

Work Rights

Not specified

Tailored Resume

Cover Letter