The Clinical Coordinator will provide clinical expertise for patients from admission to discharge and will assist in the education and development of the unit staff on the inpatient Adult General Treatment Units.
Responsible for the primary data collection and management of patient clinical information as it pertains to participation in clinical trials. Ensures timely collection of protocol related samples including shipment to outside entities as required.
The Clinical Professional Nurse Coordinator will assume responsibility and accountability for optimal clinical outcomes. The CNPC ensures optimal patient / client and family care is being delivered through a fiscally sound and safe process.
In this role, you will provide and coordinate patient care, educate patients and the public about various health conditions, and provide advice and emotional support to patients and their family members.
Responsible for coordination of Pre-Site Initiation Visits, Site Initiation Visits, Monitoring Visits, Closure Visits for all active cancer clinical trials managed in the Neely Center for Clinical Cancer Research as assigned.
In this role, you will manage the overall process and tracking of all Medicare/Medicaid case-mix documents in order to assure appropriate reimbursement for services provided within the Center. Conducts concurrent MDS reviews to assure achievement of maximum allowable RUG categories.
The Clinical Research Coordinator is responsible for managing and assisting the Principal Investigator(s) and research team in the coordination of all activities of the study as required for successful implementation of the study protocol(s).
The main responsibilities include consenting patients prior to surgery, providing the tissue bank proper notification and documentation of consent, and managing regulatory components of the neuro logic tissue banking protocols and clinical data collection and management currently open at these hospitals.