Roles and Responsibilities
The following items will be reviewed to understand the roles and responsibilities of the research team as they relate to financial compliance and clinical research:
- Budget workbook
- Delineation of PIC and RC
- Adherence to UConn Health policies
- Opening a clinical trial
- Identifying research patients
- Verirification of Continuous Monitoring Process (CMP) by study staff
Compliance/Case Review
- Assessment of compliance with (UConn Health) policies:
- Research patient billing policies and procedures
- Identification of inpatient and outpatient services
- Designation of PIC and RC
- Opening a clinical trial
- Correct billing procedure for charges
- Identification of errors and corrective plan of action
- Review may also include
- Documentation of research intervention
- Subject accrual
- Review of research records
- Review of clinic/medical records
- Assessment of compliance with State of Connecticut regulations and laws relevant to billing of patients on clinical trials.
- Assessment of compliance with federal regulations and laws relevant to billing of patients on clinical trials.
Informed Consent
- Confirm consistency between contract, protocol and approved informed consent as it relates to financial compliance.
- Confirm consistency between informed consent and actual patient charges as it relates to financial compliance.
- Review may also include:
- Dates of approval and start of research
- Changes in protocol