Clinical Research Revenue Cycle: Bridging Health Systems and Clinical Research
Instructor:
Mary Veazie
Product ID: 706775
Training Level: Beginner
- Duration: 120 Min
Why Should You Attend:
Individuals supporting the financial aspects of a clinical research study must understand the federal regulations, clinical operations and revenue cycle of a typical health system in order to be success. This course provides attendees with knowledge of the key concepts with case studies to support the learning process. We will review the pitfall and leading practice for establishing a CRRC program at a health system.
Areas Covered in the Webinar:
- Understanding a health system's revenue cycle and applicable billing regulations
- Incorporating clinical research into the health system's revenue cycle
- Understanding billing activity - billable to insurance vs. billing to sponsor
- Federal regulations underlying these concepts
- Use cases to support concepts
- Establishing clear communication between revenue cycle representatives and clinical research staff; to include why is this necessary.
Who Will Benefit:
- Research Nurses
- Study Coordinators
- Financial Analysts
- Patient Billing Specialist
- Adminstrative Managers
- Compliance Specialists
- Administrative Directors
Mary Veazie
Executive Director, Clinical Research Finance
Mary Veazie is a Certified Public Accountant with over 15 years of experience in clinical research finance. Collectively, she has over 25 years of financial and auditing experience. She developed and directed a clinical research finance office for a large academic medical center. She is certified in Healthcare Research Compliance and Healthcare Compliance. Ms. Veazie’s skill set includes full comprehension of the clinical research billing process and its impact on an organization’s clinic operations and revenue cycle.
More Training By Experts
- Financial Management of Clinical Research: Developing Data Analytics to Drive Decision Making
- Introduction to Medicare Coverage Analysis - Impact on Revenue Cycle
- Leveraging Clinical Research Processes to Decrease Denials
- Claims Processing: Appropriate Segregation of Charges & Medical Documentation for Clinical Research Studies
- Streamlining Clinical Trial Activations - Best Practice Approach
Refund Policy
Our refund policy is governed by individual products and services refund policy mentioned against each of offerings. However in absence of specific refund policy of an offering below refund policy will be effective.
Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. ComplianceOnline would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange. Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs. Substitutions can happen any time. On-Demand Recording purchases will not be refunded as it is available for immediate streaming. However if you are not able to view the webinar or you have any concern about the content of the webinar please contact us at below email or by call mentioning your feedback for resolution of the matter. We respect feedback/opinions of our customers which enables us to improve our products and services. To contact us please email [email protected] call +1-888-717-2436 (Toll Free).
