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
'403271
| Location | Philadelphia, PA |