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Important Information on CRMS Registration and Research Consent Form from the Office of the Vice Dean of Clinical Investigation 8/31/2020
Video Training for placement of Release of Information Flag (JHED ID Required - You may need to click twice)
Research Billing Buzz
Newsletter of the Johns Hopkins Medicine Office of Clinical Research Billing Compliance (CRBC)
Each month the CRBC shares with our stakeholders important and timely information related to our shared effort to ensure timely, compliant billing for research services.
A 45-minute session focused on understanding your monthly Epic RSH Account statement for services billed back to a study budget in SAP.
Online Clinical Research Billing & Revenue Cycle Resources
Notice Related to Upcoming Change to Fee Schedule Adjustment for Hospital Services Charged to Clinical Trial Budgets Effective After April 1, 2020. link to document (JHED ID Required for Access)
Hospital Facility Charge Master Files - Please contact Clinical Research Support Services at email@example.com.
This document, titled "Understanding Clinical Research Billing" is a brief primer on the workflow processes supporting billing compliance related to all activity related to participation in clinical trials across Johns Hopkins Medicine.
Clinical Research Billing Lunch & Learn Training Enrollment Request (login for LMS required)
-This interactive learning session, title "A Complete Guide to Clinical Research Billing Compliance" brings together several offices involved in the Clinical Research Revenue Cycle at Johns Hopkins and will provide you with information on what are the responsibilities of the Principal Investigator and other study team members in regards to the Clinical Research Revenue Cycle at Johns Hopkins. Our goal is to provide a foundation for understanding the key compliance related process to your studies and how CRMS and the Research Account Statement billing operate.
Clinical Research Billing & Quality Assurance
Joint Commission standards maintain that consent forms should be part of the patient’s medical record. Generally speaking, if a Hopkins patient is enrolled in a trial for which there is Hopkins IRB approval, the signed informed consent form should be added to their electronic medical record. This change in practice means that research consent forms will now be scanned into a patient’s record in Epic.
The Clinical Research Billing Compliance (CRBC) Office will scan these items in on your study’s behalf to help ensure that the scanning and indexing of the forms are completed accurately.
Clinical Research Financial Clearance
- This document explains the Insurance Clearance functionality available in CRMS. If your study has a Prospective Reimbursement Analysis,PRA, you are required to use this functionality.
Clinical Research Revenue Cycle
Clinical Research Management System (CRMS) Related Links & Material
- This link provides in-depth guidance on all facets of the CRMS application that study team members may encounter
Email contact for the CRMSHelp Team: firstname.lastname@example.org
Direct Study Billing Material
- This document explains how to enter budget numbers is CRMS. Studies with a Prospective Reimbursement Analysis, PRA, are required to enter this information in CRMS.
- This document outlines how the Direct Study Billing Process supports timely invoicing of clinical services to research study budgets.
External Agency Clinical Research Billing Compliance Related Links
Johns Hopkins University and Johns Hopkins Medicine
epic@hopkins Clinical Research Related Links
- This site contain extensive material related to Clinical Research Functionality in the epic@hopkins application
- This links directly to helpful 1 or 2 page guides to assist with many tasks within the epic@hopkins application
Last updated 8/31/2020
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