Under the guidance of Martha Weiner, Senior Director, staff working in the offices of Clinical Research Billing & Quality Assurance, Clinical Trials Financial Clearance and Clinical Research Revenue Cycle and Compliance provide support to ensure correct and compliant billing related to patient participation in research studies. Our goal is for this web page to provide relevant, up-to-date communication links and information for investigators, study coordinators and other research team personnel regarding clinical research billing for hospital and professional fee charges across the collective Johns Hopkins Medicine entities (JHU School of Medicine, JHHS Hospitals and Clinical Practice sites)
A brief description and contact information for the leadership of each office follows. Helpful documents and weblinks associated with each group are available by clicking here: Additional Resources
Associate Director: Liza Rodriguez email@example.com (410) 502-9226
CRB&QA ensures that patient care services for study participants are billed as either “routine care” [e.g., to the participant or his/her insurer] or “research only” [e.g., to be paid by the study budget / sponsor], using the Prospective Reimbursement Analysis as a roadmap. This “adjudication process” is carried out for hospital inpatient/outpatient and professional fee charges. CRB&QA is also responsible for regulatory monitoring related to clinical research billing and the association of research participant consent forms within the Epic EHR application.
Manager, Access Services Clinical Research Financial Clearance: Dawn Coleman firstname.lastname@example.org (410) 997-2115
Supervisor, Access Services Clinical Research Financial Clearance: MeChelle Baker email@example.com (443) 997-9512
CRFC staff verify insurance coverage of potential participants for outpatient studies and coordinate alongside JHM Access Services to obtain inpatient services clearance. Participants with Medicare have a defined clinical trial coverage benefit. Some insurers will refuse to pay for routine care provided in the context of a clinical trial. The Informed Consent Form of a study with a PRA explains “what will it cost” to participate in the study by referencing the Patient Financial Responsibility Information Sheet. As a result, verification prior to enrollment whether a participant’s insurance will authorize coverage is an essential element of the clinical research financial clearance process. CRFC also provides guidance for the appeal of clearance denials for routine services associated with clinical trials.
Senior Director: Martha Weiner firstname.lastname@example.org (410) 955-1861
Associate Director: Scott Streibich email@example.com (410) 502-0124
CRRC coordinates the School of Medicine components related to operational processes, planning, policies, financial management systems, monitoring and reporting on clinical research revenue cycle activities. The Clinical Research Revenue Cycle office leads planning and project management activities for the expansion of the research infrastructure support services across Johns Hopkins Medicine (JHM).