Instruction in Monitoring, Procedures Documentation and ClinicalTrials.gov (IMPACT)
Have you completed basic instruction in clinical research but are looking for more? The Instruction in Monitoring, Protocols, and Advanced documentation in Clinical Trials (IMPACT) workshop series is designed is designed for study team members who are ready for an intermediate level of training for clinical trials skills. Participants will learn critical clinical research skills through a group learning environment and hands-on skills practice. Maximum benefit will be gained by attending all three sessions, but it is not required.
ClinicalTrials.gov and Its Interaction with Protocols, Documents and Study Management
Before attending this session, participants should have either used ClinicalTrials.gov or previously attended ClinicalTrials.gov registration training from the Office of Regulatory Affairs. This session will cover new requirements for registration, updates, use of special informed consent language, results reporting, and protocol uploads. Group exercises and discussion will help participants learn how to avoid common mistakes in ClinicalTrials.gov. Topics will include how to draft arms and interventions, translating protocol aims into specific outcome measures, and results reporting for different clinical trial models.
Our aim is to provide an outstanding experience for all attendees. If you require reasonable accommodations in order to attend, please find additional information on the registration page about how to request these.