Nicole, the Clinical Research Director at RegenMed, is a dedicated clinical research professional with over 12 years of experience in the development, oversight, and implementation of clinical research projects and protocols.

Having worked as both a Senior Clinical Research Coordinator and a Clinical Research Associate, Nicole has extensive experience in both the development and monitoring of clinical trial visits. Such experience has included both investigator and industry-lead trials (Phases I/II – IV) within multiple therapeutic areas and study populations.

During her time working with community clinics, medical institutes, and government-funded agencies, Nicole has much direct experience with study patients/caregivers, study teams, and a range of physicians and research nurses. Such work has involved the development and adaptation of protocols, study assessments, SOPs, IRB processes, regulatory documentation, IP accountability, and audit preparations, with varying aims of each project.

Nicole finds passion and purpose in helping to build strong studies, with the aim of informing and protecting the rights of patients, assisting in building strong study teams with comprehensive PI oversight, while ensuring the integrity of data collected.