POSITION SUMMARY

Reports to the Manager, Clinical Trials Office and performs duties in support of the Research

Billing and Invoicing Compliance activities within the Clinical Trials Office.

POSITION DUTIES

• 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

Required:

• Bachelor s degree in healthcare, administration, or research related field.
• Master s degree in healthcare, administration, or research related field. (Preferred)
• 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.

REQUIRED KNOWLEDGE, SKILLS, AND ABILITIES

• Experience in areas of research regulatory compliance, especially related to clinical trials billing.
• Highly skilled experience and knowledge of Windows-based software required, including but not limited to Microsoft Windows, Outlook, Excel and Access.
• Possess effective time management skills to permit handling of large workload.