Clinical Research Coordinator (onsite) - Trauma Services

CoxHealth

Springfield, Missouri, United States
Onsite
Clinical research trials administration
Collecting and organizing study information
Data entry and submission timeliness
The Trauma Clinical Research Coordinator is responsible for the overall administration and operation of clinical research trials involving the Trauma Service Line

Job Summary

  • The Trauma Clinical Research Coordinator is responsible for the overall administration and operation of clinical research trials involving the Trauma Service Line.
  • This position requires knowledge of clinical protocols and good clinical practices, set forth by federal regulations and guidelines.
  • CoxHealth is a leading healthcare system serving 25 counties across southwest Missouri and northern Arkansas, recognized for workplace excellence.

Matching Summary

The Trauma Clinical Research Coordinator is responsible for the overall administration and operation of clinical research trials involving the Trauma Service Line.

Skills & Requirements

Must-have

  • Clinical research trials administration
  • Collecting and organizing study information
  • Data entry and submission timeliness
  • Maintaining research documentation
  • Working in a self-directed team environment

Nice-to-have

  • Strong organizational skills
  • Ability to multi-task
  • Prioritizing work at given timelines
  • Excellent written and verbal communication

Key Requirements

  • Bachelor's Degree in a clinical field
  • Previous experience in pre-clinical or clinical research
  • Certified as Clinical Research Coordinator

Work Rights

Not specified

Tailored Resume

Cover Letter