We are excited to introduce a series of new four interactive live classes designed to strengthen research competency and reinforce essential regulatory requirements for our research community. Tracy Graham, BSN, CCRC at Wake Forest CTSI, leads sessions focused on practical application, scenarios, and discussions, suitable for new research teammates or those needing a refresher.
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Research Informed Consent Live Class
Learn to handle ICF signature block errors, use a witness appropriately, and understand the requirements when working with participants who have Limited English Proficiency (LEP) or lack Decision-Making Capacity (DMC). Recommended prerequisite: Obtaining and Documenting Informed Consent Workday course.
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Regulatory Reporting Live Class
Practice identifying noncompliance and unanticipated problems, and review reporting requirements for local and external IRBs. Recommended prerequisite: Unanticipated Problems, Adverse Events, and Protocol Deviations Workday course.
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Safety Reporting Live Class
Develop your ability to identify and document Adverse Events (AEs) and Serious Adverse Events (SAEs) and learn best practices for AE log documentation. Recommended prerequisites: Unanticipated Problems, Adverse Events, and Protocol Deviations and Collecting and Documenting Adverse Events Workday courses.
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HIPAA in Research Live Class
Strengthen your understanding of HIPAA requirements and learn how to properly use and disclose Protected Health Information (PHI) in clinical trials research.
These classes are open to all teammates interested in research, whether you are new to the field or looking for a refresher. We encourage new researchers to complete the recommended Workday courses prior to attending the live sessions for the best learning experience.Classes are listed on the CTSI calendar and are held twice each month. For more information or to register for any of these sessions, contact Tracy Graham at Tracy.Graham@aah.org.
We look forward to seeing you there!