Job Details
*Hybrid Schedule*
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)