Study Team Member Only Change in Research (STMO CIR) Training & Information Sessions

Training and information sessions on the new Study Team Member Only Change in Research (STMO CIR) will be offered twice monthly starting in November 2024 and will run through February 2025.  The training will include a practical walk-through of how to complete the STMO CIR, review the types of study team member changes that may be submitted using this function and will discuss strategies for addressing errors that may arise in the submission process.

Sign up for a training session in MyLearning here: IRB Hot Topics: Study Team Member Only Changes In Research

If unable to attend a live session step-by-step instructions for completing the STMO CIR are available HERE.

eIRB101 is a 1 hour in-person beginners course designed to introduce new researchers to the IRB website and the JHM electronic Institutional Review Board (eIRB) System.  Topics covered include

• IRB Compliance Training Requirements
• Turn-around Time and Workflow Process
• Who's Who in the IRB
• Accounts and Websites
• Application Workspace
• Application Screens (i.e., Study Protocol, Consent Form)
• Finalizing Application and Adding Study Team Members
• Responding to IRB Issues
• Creating a Further Study Action (intro)

Please register HERE

Session dates/times: Classes are held the 3rd Friday of each month (10:00 a.m. - 11:00 a.m.)

Training Sessions: Good Clinical Practice (GCP) Fundamentals: Understanding and Applying GCP to Human Subjects Research (JHM IRB)

Good Clinical Practice or ‘GCP’ training for investigators and study-team members is increasing becoming required by institutions, sponsors, and the NIH.  This 90 minute course will explain the elements of the International Conference for Harmonization’s (ICH) principles and specific guidelines for Good Clinical Practice.  Attendees will be introduced to the GCP Principles, and will explore investigator responsibilities in human subject research, focusing on the areas of trial conduct (experience, resources, and physician duties); performance (communication with the IRB, protocol compliance, and investigational product management); ethical research (safety oversight and informed consent); and recording/reporting (data acquisition, progress summaries, and safety-event reporting).

Please register via this link: http://lms14.learnshare.com/l.aspx?CID=89&A=2&T=339728

Session dates/times: 

Classes are held the 4th Friday of each month (10:00 a.m. - 11:30 a.m.)