Program Coordinator - Ccc | Clinical Trials Office
The Ohio State University
Columbus, Ohio, US
Develop and present clinical research trainings
Ensure legally compliant research practices
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, organizing PI Orientations, developing assessments, and facilitating staff onboarding and offboarding processes.
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
Develop and present clinical research trainings
Ensure legally compliant research practices
Track training completion for system access
Onboarding and offboarding process management
Maintain staff database in RedCap
Nice-to-have
Collaborate with training manager and assistant director