In this role, you will coordinate the process for completion and transmission of the resident assessment instrument (RAI) in accordance with the regulatory requirements, including assisting with the completion of the Minimum Data Set (MDS) and Care Area Assessments (CAAs) as indicated.
In this role, you will participate in the ongoing informed consent process, ensuring that human subjects, their families, and other health care providers clearly understand what is expected of and from them in the course of participating in a clinical/translational trial.
In this role, the selected candidate will manage screening, consent volunteers, maintains accurate and timely documentation and communication with volunteers, research nurse and investigators, participants, IRB and other research related entities.
In this role, the selected candidate will perform packaging and ships study specimens (blood, urine, etc.) to the sponsor or laboratory in accordance with sponsor and shipping guidelines and regulations, maintaining appropriate documentation.
As a Clinical Coordinator at DaVita you will have the opportunity to excel as the superior dialysis nurse, mentor and clinical expert you are-and have a dramatic impact on the lives of our patients and their families.