Archive: Clinical Research Financial Management for Investigative Sites
Course Description
Frequently, clinical research financial regulations, the budget process, clinical trial revenue cycle, and patient remuneration are obscure topics to not only the investigator, but also to the study team delegates. This web seminar describes the significance of ensuring that the investigator and study team are integrated into the financial components of the study to mitigate the risks associated with non-compliance with federal research billing regulations. Strategies for developing operational efficiencies and establishing communication channels to enhance sponsor reimbursements while reducing insurance denials will also be discussed.
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Learning Objectives
- Describe the significance of incorporating the investigator and study team into the financial phases of a clinical study
- Discuss the importance of integrating the development and approval of the protocol with the budget/contract process
- Discuss the impact of sponsor data capture systems, vendors, monitors, and auditors on clinical trial financial milestones
- Describe standard operating procedures and communication channels required for compliant clinical study financial billing (sponsor /patient), insurance authorizations, and participant remuneration
Who Should Attend
- Clinical Research Coordinators
- Clinical Trial Managers
- Clinical Research Associates
- Clinical Research Managers/Directors
- Administrative Directors
- Financial Analysts
- Research Nurses/Research Nurse Manager
Instructor
Mary L. Veazie, M.B.A., CPA, CHC, CHRC
Click here for complete trainer biographies
Hold this course at your company! For more information, contact Naila Ganatra at +1 215.413.2471.
