Narvelle Delabruere, BS, MSc, CCRA, CCRP is an instructor in the Foundations of Clinical Research Program.
She is a research professional with more than 15 years of clinical site and industry experience. She has led phase I-IV medical device and pharmaceutical studies across a plethora of medical therapies including interventional cardiology, gastroenterology, endocrinology, oncology, peripheral vascular, neurovascular, and gynecology.
Narvelle’s experience includes various site roles in which she engaged in budget and contract negotiations, consenting of research participants: children, adults, and legally authorized representatives, source creation, Institutional Review Board submissions, data collection, data entry, adverse event reporting, investigational product distribution and accountability, regulatory binder maintenance, specimen collection, preparation, and shipping. Her industry experience is vast as she has supported clinical trials from inception to regulatory approval. She has participated in study design and essential document development including protocol, case report forms, monitoring plan, safety management plan, and the statistical analysis plan.
She earned a Bachelor of Science in Public Health from San Diego State University and a Master of Science in Clinical Research Administration from Walden University. She is a Certified Clinical Research Associate (CCRA) through the University of California San Diego Extension Program in Clinical Trials Design and Management. She is also a Certified Clinical Research Professional (CCRP) through the Society of Clinical Research Associates and a Certified Clinical Research Associate (CCRA) through the Association of Clinical Research Professionals (ACRP).