United States of America
John has worked in the health care industry his entire career and has broad-based experience in clinical research and pharmaceutical manufacturing, regulatory strategy and compliance, and quality management. John has overall management responsibility for Beaufort’s quality oversight and clinical trial monitoring practices. As a member of Beaufort’s senior management team, he also has a leadership role in identifying and developing high-quality, customized solutions to clients’ regulatory, clinical development, quality management and manufacturing needs. These activities include clinical development and study design, clinical trial management, inspection readiness, regulatory submissions and cGMP and cGCP support.