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This MGB Human Research Affairs (HRA) course is for investigators and all members of the study staff. Course content is based on Good Clinical Practice (GCP), federal and state research regulations, and institutional research policies. Although many research teams require this comprehensive informed consent 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 consenting human subjects.
— Attendance is tracked through Zoom and cross-referenced with registration in HealthStream. If users do not meet attendance requirements, then they will not receive a Certificate of Completion in HealthStream.
— Re-certification may be required by MGB HRA IRB or the MGB HRA Compliance & Education office.
— Future dates can be found on HealthStream or on our Brigham calendar.
— Search “MGB HRA” to find all courses.
— Please also see notes above on RCR credit.
— The recorded (“on-demand”) version can be found on HealthStream.
— Search “MGB HRA” to find all courses.
— Please also see notes above on RCR credit.