Clinical Oncology Research Coordinator- RN- Columbus-40hrs

GENERAL SUMMARY:

Performs nursing functions independently and in collaboration with physician investigator to ensure that the objectives of an established research protocol are met and in compliance with IRB and sponsor guidelines. Identifies and recruits patients into study protocols as needed. Provides for educational and/or emotional support to patients enrolled in the study protocol. Is responsible for managing the study documentation and data collection for the study, and preparing and monitoring the budgets as needed. Supports physician investigators and other clinicians as necessary to facilitate project participation and compliance.