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The Office of Research and Scholarship:
Assistance is also available to help researchers navigate and complete the electronic online application – CICERO – and prepare the IRB application for continuing review, protocol amendments, and Reportable New Information (RNI).
Jessica Rowe, MS, MA, CCRP is UMSON's research quality improvement specialist. She can:
Rowe also serves as the UMSON IRB signatory, conducting departmental reviews prior to IRB review. This includes reviewing all human subject research applications submitted via CICERO.
For any IRB and regulatory questions or concerns or to request training and/or a quality assurance assessment, please contact Jessica Rowe at email@example.com or 410-706-1611.
When conducting human subjects research at UMSON, you are required to complete:
All employees that work in a laboratory are required to complete Environment Health and Safety training (EHS).
Research team members must keep Basic CITI, HIPAA, and GCP completion reports/certificates on file. These records should be placed in appropriate study binders, if applicable. Students involved in human subjects research are required to submit completion reports to the principal investigator of the study and to the associate dean of their degree program.
UMSON employees and affiliates actively engaged in human subjects research are required to submit initial documentation of GCP training to:
The Office of Research and Scholarship offers a Monthly Research Seminar Series on various topics.