Clinical Research Coordinator I - Ri Behav Trials Off

Nationwide Children's Hospital

Columbus, OH, United States
Ich/gcp guidelines
Subject recruitment and consent
Data collection and management
The Clinical Research Coordinator I manages elements of a clinical study in order to meet all protocol obligations while following ICH/GCP guidelines and departmental/institutional standard operating procedures

Job Summary

  • The Clinical Research Coordinator I manages elements of a clinical study in order to meet all protocol obligations while following ICH/GCP guidelines and departmental/institutional standard operating procedures.
  • Essential functions include recruiting, consenting, and enrolling subjects, ensuring they meet inclusion/exclusion criteria, and collecting and managing research data.
  • The role requires adherence to departmental quality control guidelines, completion of Case Report Forms, and maintenance of the regulatory binder and documents.

Matching Summary

The Clinical Research Coordinator I manages elements of a clinical study in order to meet all protocol obligations while following ICH/GCP guidelines and departmental/institutional standard operating procedures.

Skills & Requirements

Must-have

  • ICH/GCP guidelines
  • Subject recruitment and consent
  • Data collection and management
  • Specimen processing
  • Regulatory binder maintenance

Nice-to-have

  • Patient/family advocate
  • Team player
  • Goal-oriented and self-directive

Key Requirements

  • Associates degree or equivalent experience
  • Ability to obtain CRA/CRC certification
  • Understanding of medical terminology
  • Working knowledge of PCs and software

Work Rights

Not specified

Tailored Resume

Cover Letter