Essentials for Regulatory Specialists: A new virtual workshop

CTSI is now offering a virtual workshop that provides training for University of Minnesota research professionals, such as regulatory specialists, research coordinators, project managers, who are new to taking on a regulatory role in human research studies.

Curriculum

The workshop covers:

• The role and responsibilities of a regulatory specialist
• The regulations that define their role 
• Creating consent forms and other essential study documents 
• Maintaining a regulatory binder 
• IRB submissions

This a four-hour training over two days. 

Prerequisites

To take the course, participants must complete the following required training prior to attending: :

• HIPAA training
• CITI training - Good Clinical Practice (GCP) and Human Research Protections for Biomedical Study Teams training or Social/Behavioral or Humanist Research Investigators and Key Personnel

Take the course

The course will be offered quarterly, and is available for self-registration through the University of Minnesota’s Training Hub. 

Access the training