Clinical Research Coordinator I - Ri Behav Trials Off

stantonlab.info

Ich/gcp guidelines
Subject recruitment and enrollment
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

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.
  • Essential functions include recruiting, consenting, and enrolling subjects, collecting and managing research data, and preparing and processing human specimens.
  • The role requires adherence to departmental quality control guidelines and maintaining regulatory binders 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.

Skills & Requirements

Must-have

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

Nice-to-have

  • Patient/family advocacy
  • Quality control adherence
  • Team player attitude

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