Clinical Research Coordinator I - Ri Gastroenterology
Nationwide Children's Hospital
Ich/gcp guidelines
Protocol obligations
Subject recruitment and consent
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, collecting and managing research data, preparing and processing human specimens, and collaborating with other hospital services.
This role requires an Associate's degree or equivalent work experience, with a BA/BS preferred, and the ability to obtain CRA/CRC certification.
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.