Clinical Research Coordinator 4

Vanderbilt University Medical Center

Nashville, Tennessee, United States
Hybrid
5 years relevant research experience
Socra certification required at hire
Pediatric clinical research experience
This role leads day-to-day operations of the multi-site DOSE Trial with minimal supervision while ensuring high-quality study conduct and regulatory compliance

Job Summary

  • This role leads day-to-day 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 take exceptional pride in advancing health through world-class research.

Matching Summary

This role leads day-to-day 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 certification required at hire
  • Pediatric clinical research experience
  • IRB submission and review experience
  • Multi-site study coordination
  • Team supervision and leadership

Nice-to-have

  • Spanish language skills preferred
  • REDCap database development expertise
  • Manuscript and grant writing support
  • Culturally responsive communication
  • Hybrid remote work flexibility

Key Requirements

  • Bachelor's Degree or equivalent experience
  • Certified Clinical Research Professional (SOCRA)
  • Minimum 5 years of relevant research experience
  • Previous IRB experience required
  • Experience working with Pediatrics

Work Rights

Not specified

Tailored Resume

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