Program Coordinator - Ccc | Clinical Trials Office
The Ohio State University
Columbus, Ohio, US
Legally compliant and ethical research practices
Develop and present clinical research trainings
Track training completion for system access
The Program Coordinator will serve as a resource to promote and ensure legally compliant and ethical research practices within the Clinical Trials Office (CTO) and Comprehensive Cancer Center (CCC)
Job Summary
The Program Coordinator will serve as a resource to promote and ensure legally compliant and ethical research practices within the Clinical Trials Office (CTO) and Comprehensive Cancer Center (CCC).
Responsibilities include developing, coordinating, managing, and presenting trainings related to the conduct of clinical research, including FDA Regulations, ICH Guidelines, and NCI requirements.
The role involves assisting with training on software systems, coordinating training sessions, facilitating staff onboarding, and maintaining databases and communication channels.
Matching Summary
The Program Coordinator will serve as a resource to promote and ensure legally compliant and ethical research practices within the Clinical Trials Office (CTO) and Comprehensive Cancer Center (CCC).
Skills & Requirements
Must-have
Legally compliant and ethical research practices
Develop and present clinical research trainings
Track training completion for system access
Coordinate training sessions and onboarding
Maintain staff database and SharePoint site
Nice-to-have
Collaborate with leadership
Provide direct feedback and guidance
Facilitate key aspects of onboarding
Key Requirements
Bachelor’s Degree or equivalent experience
One year of clinical research experience
Knowledge of GCP and federal regulations preferred