Clinical Research Coordinator I - Ri Pulmonary

Nationwide Children's Hospital

Main Campus, OH, United States
Ich/gcp guidelines
Protocol obligations
Data collection
The Clinical Research Coordinator I manages elements of a clinical study 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 to meet all protocol obligations while following ICH/GCP guidelines and departmental/institutional standard operating procedures.
  • Responsibilities include recruitment, consent, enrollment, data management, specimen processing, and maintaining regulatory binders.
  • The role requires adherence to institutional IRB, federal, and state regulations, and collaboration with other hospital services and the PI/sub-I.

Matching Summary

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

Skills & Requirements

Must-have

  • ICH/GCP guidelines
  • protocol obligations
  • data collection
  • subject recruitment
  • specimen processing
  • regulatory binder maintenance

Nice-to-have

  • patient/family advocate
  • team player
  • goal-oriented
  • self-directive

Key Requirements

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

Work Rights

Not specified

Tailored Resume

Cover Letter