About this role
Schedules all Research Participants (RPs) enrolled in protocols managed by the Office of Clinical Research (OCR) during the screening, active treatment, and follow up phases of study participation. Collaborates with the Clinical Research Coordinator, Clinical Research Nurse, Clinical Research Associate, and Clinical Trials Financial Counselor to ensure that Research Participants are scheduled in a timely manner while complying with the requirements of the protocol and study budget.
Education High School Diploma or Equivalent Required
Experience 3 years experience in a healthcare/hospital environment Required General Experience in Insurance or Billing Preferred General Experience with and understanding of Clinical Trials Preferred
Licenses