Kelsey Lecesse, CphT

Regulatory Affairs
As MBR’s regulatory coordinator, Kelsey is responsible for regulatory submissions to institutional review boards and study sponsors. Through her work, Kelsey encourages a timely and efficient study start up process and ensures patient safety through GCP/Regulatory compliance over the course of a clinical trial.
Kelsey Lecesse – Monroe Biomedical Research - Monroe Biomedical Research
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