This presentation will focus on lessons learned from a recent observational study of 6 clinical research sites over the course of three years. The logistics of database management, study operations, training and compliance, invoice tracking and financial considerations, authorship and publication guidelines, marketing and recruitment materials, and more. All clinical research site roles are encouraged to attend.
Upon completion of this Webinar, attendees should be able to:
Discuss the roles and responsibilities involved in a Multi-Centered Investigator-Initiated Trial.
Review specific considerations when the site becomes the sponsor of an IIT.
Share best practices for logistics based on the experience of a six-sites IIT.
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