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, tracking training completion, organizing PI Orientations, and developing/reviewing assessments to ensure comprehension.

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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
• Computer literacy with Microsoft Office software
• Clinical research certification from SOCRA or ACRP desired
• Experience in presenting training programs desired

Work Rights