Job Title

*Hybrid Schedule*OverviewFacilitate audit of ongoing clinical trials for accuracy and compliance with applicable policies, regulations and laws. Prepare reports outlining findings and corrective and preventive action plans.Works closely with Revenue Cycle teams to resolve clinical research billing errors.Analyzes billing errors to identify root causes and executes work plans to correctidentified deficiencies.Ensure timely and accurate clinical trial invoicing as assignedInvoice all active clinical trials consistent with contract termsActs as a resource in the development of internal policies, procedures and jobaides related to clinical trial invoicing .Act as a resource in patient care billing compliance, participating in training andeducation as needed.Acts as a resources in the development of internal policies, procedures and job aidesrelated to clinical trial billing.Responsible conduct of research at all times. 3-5 Must Have SkillsQualificationsBachelor's degree in healthcare, administration, or research related field.Three years or more of experience working in a clinical research environment including astand-alone research site, a research department, or in research administration such as a centralized research office, or with an institutional review board.Experience in areas of research regulatory compliance, especially related to clinical trials billing. (Familiar with CPT Codes, NCDs and LCDs)Highly skilled experience and knowledge of Windows-based software required, includingbut not limited to Microsoft Windows, Outlook, Excel and Access.Direct Hospital Revenue andor Clinical Research Background (focus on CR first)