Dr. Constance Cullity is Senior Director, Regulatory Compliance at Advarra. Her expertise is in the areas of human subject protection (HSP) and good clinical practice (GCP) regulatory compliance. Among her duties, Dr. Cullity serves as a member of Advarra’s regulatory leadership, provides regulatory guidance to staff and clients, and delivers internal and external training. Before joining Advarra, she completed a career in federal service, serving more than 20 years with the U.S. Food and Drug Administration (FDA). During her lengthy career at FDA, she held several positions, including as a Supervisory Medical Officer and the Associate Director for Human Subject Protection in FDA’s Center for Drug Evaluation and Research (CDER) and as a Branch Chief in GCP Compliance Divisions. As a Branch Chief, Dr. Cullity oversaw the full spectrum of CDER’s GCP regulatory compliance activities related to clinical-trial conduct and served as an HSP expert. She graduated from Kean College, obtained her medical degree from Robert Wood Johnson Medical School, and attended post-graduate medical training in psychiatry at Yale University. She also holds a Master of Public Health degree from Johns Hopkins University Bloomberg School of Public Health. 

Constance Cullity is an expert in the areas of human subject protection and Good Clinical Practice regulatory compliance, having served more than 20 years with the FDA.