Presenter

Emilea is a Consultant Biostatistician specializing in clinical trial data and regulatory reporting across medical device and drug development. She supports sponsors in aligning study design and statistical outputs with regulatory expectations, audit readiness, and operational clarity. Emilea has led development of automation tools to support data management, analysis plan writing, CDISC dataset creation, and Clinical Study Reports. Her interest in automation is to help the end-user focus on the development of their product.