Executive Director, Global Quality Assurance & Compliance
Lorrie D. Divers has worked in clinical trials for 25 years in both the pharmaceutical and medical device industries, as well as in academic research centers. Her previous positions cover the spectrum of clinical research activities, from study coordination, data management, and program coordination to monitoring, clinical project management, quality assurance, and process improvement/Lean Six Sigma. She has nine years of experience in GCP quality assurance, compliance, and training and has successfully managed numerous regulatory authority inspections in the site, sponsor, and central laboratory arenas. Lorrie has presented on GCP topics at local and national SoCRA meetings, as well as at investigator meetings, and has delivered numerous corporate training sessions on clinical research topics. She is a Certified Clinical Research Professional (SoCRA) and a Registered Quality Assurance Professional in GCP (SQA).