Skip Navigation

Clinical Research Management System (CRMS)


Assists clinical research staff and associated administration groups with the management of human subjects research studies. The study and participant registry tracks information about all studies and the participants on those studies.  CRMS interfaces with the Electronic Institutional Review Board (eIRB) system so that the study registry is automatically kept up-to-date.  Additional CRMS features are eligibility checklists, consent form tracking, study document management, canned reports, and adhoc queries on a data warehouse.  We are currently developing additional features to support electronic protocols, electronic case report forms, and streamlined insurance clearance.

Clinical Leaders

Dr. Dan Ford, Dorothy Damron

Technical Leaders

Diana Gumas, Samuel Dongmo

Current Status

Study and Participant registry is fully installed at Johns Hopkins Hospital and Bayview Medicine for use on Johns Hopkins School of Medicine studies. The system is upgraded quarterly.