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 and presenting at CTO PI Orientation, and developing assessments to ensure comprehension of research concepts.

Matching Summary

Skills & Requirements

Key Requirements

• Bachelor’s Degree or equivalent
• One year clinical research experience
• Good clinical practice guidelines knowledge
• Federal regulations knowledge
• Microsoft Office proficiency
• Clinical research certification desired
• Presenting training programs experience desired

Work Rights