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 and Comprehensive Cancer Center by developing, coordinating, managing and presenting trainings related to the conduct of clinical research.
• Responsibilities include presenting trainings on general research topics, assisting with training on software systems, and coordinating the CTO PI Orientation for new physicians.
• The role involves assessing comprehension of research concepts through assessments and assignments, providing feedback, and facilitating staff onboarding and offboarding processes.

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Skills & Requirements

Key Requirements

• Bachelor’s Degree or equivalent combination of education and experience
• One year of experience in a clinical research capacity
• Knowledge of good clinical practice guidelines
• Knowledge of federal regulations
• Computer literacy with Microsoft Office software

Work Rights