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Clinical Research Revenue Cycle Coordinator II
4 months ago
Overview
- Facilitate 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 correct
identified deficiencies. - Ensure timely and accurate clinical trial invoicing as assigned
- Invoice all active clinical trials consistent with contract terms
- Acts as a resource in the development of internal policies, procedures and job
aides related to clinical trial invoicing .
- Act as a resource in patient care billing compliance, participating in training and
education as needed. - Acts as a resources in the development of internal policies, procedures and job aides
related to clinical trial billing. - Responsible conduct of research at all times.
3-5 Must Have Skills/Qualifications
- Bachelor's degree in healthcare, administration, or research related field.
- Three years or more of experience working in a clinical research environment including a
stand-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, including
but not limited to Microsoft Windows, Outlook, Excel and Access. - Direct Hospital Revenue and/or Clinical Research Background (focus on CR first)