Clinical Research Coordinator I - Ri Behav Trials Off
Nationwide Children's Hospital
Not specified; not specified; not specified
Ich/gcp regulatory compliance knowledge
Subject recruitment and enrollment skills
Accurate data collection and documentation
The Clinical Research Coordinator I manages all elements of a clinical study to ensure protocol obligations are met while adhering to ICH/GCP guidelines
Job Summary
The Clinical Research Coordinator I manages all elements of a clinical study to ensure protocol obligations are met while adhering to ICH/GCP guidelines.
Essential duties include recruiting and consenting subjects, collecting biological samples, performing CLIA waived lab tests, and maintaining accurate regulatory binders.
Candidates must possess an Associate degree or equivalent experience and demonstrate the ability to obtain CRA/CRC certification in a timely manner.
Matching Summary
The Clinical Research Coordinator I manages all elements of a clinical study to ensure protocol obligations are met while adhering to ICH/GCP guidelines.
Salary
Not specified; Not specified; Not specified
Skills & Requirements
Must-have
ICH/GCP regulatory compliance knowledge
subject recruitment and enrollment skills
accurate data collection and documentation
human specimen collection and processing
CLIA waived laboratory assessments
Case Report Form (CRF) completion
Nice-to-have
patient and family advocacy experience
strong analytical and organizational skills
ability to work evening and weekend hours
team player with excellent communication
goal-oriented and self-directive attitude
Key Requirements
Associates degree, STNA, PCA, LPN, MA or equivalent experience
BA/BS preferred
Ability to obtain CRA/CRC certification
Previous clinical research or healthcare experience preferred