Your Research Roadmap: From Idea to IRB Approval

This session will guide graduate students and postdoctoral scholars through the process of transforming a research question into a well-designed human subjects study. We'll explore key considerations in study planning, participant protections, informed consent, and the IRB review process. Participants will gain practical tips for developing stronger protocols and avoiding common submission pitfalls. We'll also discuss how the IRB serves as a collaborative partner in supporting ethical, impactful research. Whether you're planning your first study or preparing for future projects, you'll leave with a clearer understanding of the path from idea to implementation. Bring your questions and research ideas as we map out the journey together. This seminar is lead by Vivienne Carrasco, MPH, CIP, Associate Director of Regulatory Affairs with the University of Miami's Human Subjects Research Office.