The July 2021 Clinical Research Staff Quarterly Training will focus on hot topics in IRB and research compliance.
Big changes are coming to IRB forms and submission processes. Join us on July 15 for the next session of the Tufts Medical Center (Tufts MC) and Tufts CTSI Professional Education Clinical Research Staff Quarterly Training series. You’ll get the inside scoop on what is new, what you will be required to do, and best practices for working with the Tufts IRB. If you are involved in study start-up activities or interact with research participants or IRB submissions, these sessions are for you! These quarterly trainings are also a great way to get connected to the community of clinical research professionals at Tufts MC.
The July session continues our focus on topics in research compliance specific to Tufts MC. Whether you are an experienced coordinator, or new to Tufts MC, there will be something here that is relevant to your work.
Christine Choy, IRB Supervisor and Database Administrator
Caitlin Farley, IRB Administrator II
Carly Tucker, Clinical Research Compliance Manager
Diversity Enrollment, Biospecimen Banking, and More
The IRB office recently updated their forms and templates to reflect new processes to highlight and improve enrollment of diverse populations, their updated Biospecimen banking (formerly tissue banking) policy, and much more. You will learn about all of these changes; which forms, templates, and policies were revised, created, and eliminated; and how these changes will affect current and new studies.
Best Practices for IRB Submissions and Responding to IRB Comments
The IRB office will provide tips and guidance for a smooth and efficient IRB review of your projects. You will learn best practices for submitting studies to the Tufts IRB, responding to comments and requested revisions, and getting your study approved as quickly as possible.
Third Party Vendor Risk Assessment Update
This short update will cover the EVA page for approved research vendors including: where to find the list, how to best understand and use the approved vendors list, and other tips and tricks for this new vendor review.
Who should attend
Clinical research staff are encouraged to attend.
Thursday, July 15
Online via Zoom (a link will be sent to those who register).