CFRI is dedicated to furthering the research that promotes Le Bonheur’s mission in preventing, treating and eliminating childhood disease. Our team members are available to provide support for Le Bonheur researchers. Our staff can assist with grant preparation, navigating research regulations, setting up clinical trials, requesting chart reviews, biostatistics, biomedical informatics and medical editing and writing.
Who are you?
We are the Regulatory Core team. Our staff includes Research Regulatory Manager Dalia Aguilar-Canseco, Clinical Research Coordinator Rose Prince and Clinical Research Coordinator Jehad Webb.
What can you do for researchers?
We can provide support for researchers in many ways, including preparing research projects, assisting with reviewing IRB applications prior to submission, helping answer and/or address provisos, completing and submitting IRB forms (upon request), obtaining Methodist Le Bonheur Healthcare (MLH) institutional approval, providing guidance and tools to meet regulatory requirements, reviewing study records and providing recommendations prior to audits by the IRB and FDA and guiding researchers through the process of using external IRBs.
How can researchers contact your team?
Feel free to contact any member of our team:
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