Department of Pediatrics

Barbara is our Clinical Trial Research Nurse expert with twenty years of experience  in clinical trials and IRB processes. She will work directly with faculty; one-on-one or in a group. Along with her Research Assistant, there is also limited support of direct study functions such as assisting with study coordination, enrolling participants and specimen processing.

What Barbara can offer instruction in:

• protocol development
• IRB: submissions, amendments, continuing reviews, deviations, adverse events, and termination
• contract and budget support
• Clinical Trial  coordination, consent process, recruitment and enrollment , monitoring and problem resolution