Clinical Research Coordinator I - Ri Gastroenterology
stantonlab.info
Ich/gcp guidelines
Patient/family advocate
Collect and manage research data
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.
This 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
patient/family advocate
collect and manage research data
prepare human specimens
complete Case Report Forms
Nice-to-have
understanding of medical terminology
goal-oriented and self-directive
actively participate as a team player
Key Requirements
Associates degree or equivalent experience
Ability to obtain CRA/CRC certification
Previous experience in clinical research or healthcare