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) by developing, coordinating, managing and presenting trainings related to the conduct of clinical research.
• Responsibilities include collaborating with the CTO Training Manager to update trainings, independently presenting general research topics, and assisting with training on software systems for internal teams and external monitors.
• The role involves organizing and presenting at the CTO PI Orientation, developing and reviewing assessments to provide feedback, and maintaining relationships with CTO staff to assess training needs and ensure successful onboarding.

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Skills & Requirements

Key Requirements

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

Work Rights