The Clinical Research Coordinator 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 manages all elements of a clinical study to ensure protocol obligations are met while adhering to ICH/GCP guidelines.
Responsibilities include recruiting subjects, obtaining informed consent, collecting biological samples, and maintaining accurate regulatory documentation.
The role requires collaboration with hospital services and the Principal Investigator to schedule visits and ensure subject safety.
Matching Summary
The Clinical Research Coordinator 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 regulations compliance
subject recruitment and consent
accurate data collection and management
human specimen preparation and handling
CLIA waived laboratory assessments
Case Report Forms completion
Nice-to-have
patient and family advocacy skills
strong analytical and organizational abilities
team player with self-directive nature
excellent verbal and written communication
experience in pediatric pulmonary research
Key Requirements
Associates degree or equivalent experience
STNA, PCA, LPN, MA, or BA/BS preferred
Ability to obtain CRA/CRC certification
Previous clinical research or healthcare experience preferred