Clinical Research Revenue Cycle Coordinator II

*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)