Clinical Research Coordinator I - Ri Gastroenterology

Nationwide Children's Hospital

Main Campus, OH, United States
Ich/gcp guidelines
Protocol obligations
Subject recruitment and consent
The Clinical Research Coordinator I manages all aspects of clinical studies, from start-up to closure, ensuring adherence to protocol obligations and regulatory guidelines

Job Summary

  • The Clinical Research Coordinator I manages all aspects of clinical studies, from start-up to closure, ensuring adherence to protocol obligations and regulatory guidelines.
  • Responsibilities include recruiting and consenting subjects, collecting and managing research data, processing human specimens, and maintaining accurate study documentation.
  • This role requires strong organizational, communication, and analytical skills, with a focus on subject safety and data integrity.

Matching Summary

The Clinical Research Coordinator I manages all aspects of clinical studies, from start-up to closure, ensuring adherence to protocol obligations and regulatory guidelines.

Skills & Requirements

Must-have

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

Nice-to-have

  • patient and family advocacy
  • quality control adherence
  • team player attitude
  • analytical and problem-solving skills

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