Summary:

This course is for investigators and all members of the study staff conducting clinical research visits virtually. Course content is based on Good Clinical Practice Guidelines, federal and state research regulations, and institutional research policies. Although many research teams require this comprehensive course as part of onboarding, it is also a great refresher for experienced members of the study team to ensure they are aware of the most current research regulations, institutional policies, and best practices for conducting clinical research.

Sample of Topics:

• Electronic Signatures
• Protocol Procedures
• Virtual Visits Informed Consent
• Interactions with Sponsors

Speakers:

• Pamela Richtmyer – Director, MGB Human Research Affairs Compliance & Education Office
• Kathy Vernovsky – MGB Human Research Affairs Compliance & Education Office

Additional Details:

• The Virtual Clinical Research training will be offered every other month through the MGB Human Research Affairs Compliance & Education Office. Future dates can be found here.

**This session will be held virtually. The link will be sent to those who register with a BWH/MGB-affiliated email address ~1 day prior to the session**

CLICK HERE TO REGISTER