Clinical Research Coordinator - Radiation Oncology

Clinical Research Coordinator to coordinate and perform daily clinical research activities in accordance with approved protocols administered by the Department of Radiation Oncology. 

This position will be required to be in the office 5 days per week with a Monday-Friday work schedule. Work locations include The James Cancer Hospital and Stephanie Spielman Comprehensive Breast Center.

Responsibilities:  

• Research involving registration of patients, scanning and filing study consents, collecting patient data, for the clinical research trials in Radiation Oncology Department. 

• This will include collection of current study participant information, as well as up keeping and maintenance of already collected patients information over time, to update their outcomes and survival, as well as additional molecular data.  

• Assists with assessing patient records to identify patients who are eligible to participate in specified clinical research protocols

• Recruits, interviews and enrolls patients

• Obtains informed consent and ensures consent process is administered in compliance to regulatory and sponsor requirements

• Educates patients and families of purpose, goals, and processes of research study

• Supports activities to ensure compliance with all Institutional Review Boards (IRB), FDA (Federal Drug Administration), federal, state and industry sponsor regulations

• Assists with coordinating and preparing for external quality assurance and control reviews by IRB, federal or industry sponsors

• Participates in activities to develop new research protocols and contributes to establishment of study goals to meet protocol requirements

• Upkeep of regulatory documents for clinical trials.

• Collection, processing, transporting of select biological samples for research trials.

• Other duties as assigned