3-hr Virtual Seminar: Building a Process for Clinical Trial Billing That Works

This 3-hour training will explain how to devise a clinical trial billing system or process to manage the billing of clinical trial charges in compliance with Federal rules and regulations.

Who will benefit:

This 3-hour course will provide valuable assistance to all personnel involved in the research enterprise, including:

• Clinical Trial Sponsors
• Research Institutional Leaders
• Research Compliance professionals
• Clinical Research Professionals
• Clinical Trial Billing/coding professionals

Instructor Profile:

Bob Romanchuk, is a clinical research professional with over 15 years of experience in a broad range of clinical research infrastructure building, operation and management of both IRBs and research programs. This includes assembling and managing an IRB, building a cardiovascular research center for a large community hospital and the creation and operation of a central research office for a 13 hospital system across North Carolina, South Carolina and Virginia. His certifications include CIP (Certified IRB Professional), CHRC (Certification in Health Research Compliance), CCRC (Certified Clinical Research Coordinator) and CCRCP (Certified Clinical Research Contract Professional). He has presented numerous times nationally on the subjects of clinical trial billing, human subjects protections and the creation and operation of centralized research offices.