In this role, you will establish and maintain research files and documentation pertaining to regulatory requirements for clinical trials. Attends weekly research team meetings and updates staff and investigators on the status of regulatory submission and amendments.
The Clinical Appeals Review Coordinator is responsible for the review of medical records and development of appeals for medical necessity denials related to revenue integrity audits and other medical necessity denials as requested for all CHS affiliated hospitals.
In this role, the selected candidate will be responsible for planning and management of the approval, implementation and conduct of research protocols from planning through completion and reporting, assuring that the processes, integrity and quality of the research are assessed and maintained and that the trial is conducted in accordance with Good Clinical Practice Guidelines, federal and sponsor regulations and guidelines, Vanderbilt Policy and Procedure and research protocols.
In this role, you will serve as clinical resource. Provides/assists in direct care when appropriate to complex patients. Consults physicians and other healthcare providers to communicate patient progress.