Over 25 years of experience in clinical research operations at top tier academic medical centers with 20 years in progressive leadership roles. Extensive knowledge of research regulations and clinical operations as well as expertise in developing policies and procedures to increase compliance and reduce organizational risk. Extensive experience with regulatory submissions, developing and scaling research programs, federal audits, training clinical and non-clinical stakeholders, managing large cross-functional teams, developing policies and SOPs, and management of up to 15 independent, concurrent clinical trials. Experienced public speaker and writer with co-authorship on 8 published articles in peer-reviewed journals.