(Virtual: Zoom) ClinicalTrials.gov Training | Registration and Results Reporting
March 17 @ 1:00 pm - 2:30 pm
**This session will be held virtually on Zoom. The link will be sent to those who register with a BWH/MGH/MGB-affiliated email address ~1 day prior to the session**
Speakers:
Pamela Richtmyer – Director, MGB Human Research Quality Improvement (QI) Program
Kathy Vernovsky – MGB Human Research Quality Improvement (QI) Program
Join the MGB Human Research Quality Improvement Program for ClinicalTrials.gov technical training. This session is offered to investigators and study staff to provide the tools to navigate the ClinicalTrials.gov database proficiently and ensure compliance with current regulatory requirements.
The workshop will include a practical summary of current regulatory requirements and consequences of noncompliance, technical training to complete the registration and results reporting modules, and tips and considerations to avoid common errors. A live walk through a test record in the database will be included.
Target Audience: Investigators and study staff who are conducting clinical trials and need to register on ClinicalTrials.gov.
The ClinicalTrials.gov training will be offered every other month. Future dates can be found here.
RCR Eligibility: Completion of this session fulfills 1 of the 4 hours outlined in part 3 of the RCR requirement (hospital-based lectures).