Clinical Research Coordinator Ii - Ri Behav Trials Off
stantonlab.info
OH, United States
On-site
Ich/gcp guidelines
Subject safety
Protocol adherence
The Behavioral Trials Office is seeking a Clinical Research Coordinator II to manage behavioral-focused clinical studies, ensuring adherence to protocols and ethical guidelines. The role involves coordinating study activities, training staff, and maintaining regulatory compliance. Candidates should possess relevant experience in clinical research, effective communication skills, and the ability to work independently
Job Summary
The Behavioral Trials Office (BTO) supports the mission of providing efficient coordination of diverse behaviorally-focused clinical research across various pediatric departments.
Manages elements of a clinical study from start-up to closure, ensuring protocol obligations are met and adhering to ICH/GCP guidelines.
Conducts clinical studies, recruits and consents subjects, coordinates study visits, manages data, and assists with scientific publications and grant proposals.
Matching Summary
Match Score: 85
The Behavioral Trials Office is seeking a Clinical Research Coordinator II to manage behavioral-focused clinical studies, ensuring adherence to protocols and ethical guidelines. The role involves coordinating study activities, training staff, and maintaining regulatory compliance. Candidates should possess relevant experience in clinical research, effective communication skills, and the ability to work independently.
Skills & Requirements
Must-have
ICH/GCP guidelines
subject safety
protocol adherence
data collection and management
regulatory compliance
Nice-to-have
team player
goal-oriented
self-directive
Key Requirements
Associate's degree or equivalent experience
Eighteen months experience in clinical research or health care