David S. O’Connor
Associate Director in the Science and Technology practice at Lachman Consultants and an accomplished Quality Assurance professional with over twenty years of experience in pharmaceutical research from both a sponsor and Contract Research Organization (CRO) perspective. He has extensive QA experience in all aspects of Clinical (GCP) and Preclinical (GLP) studies and experience with Manufacturing (GMP) Quality Assurance responsibilities in R&D solid-dose formulations. He delivers leadership in the preparation, coordination and follow-up of regulatory inspections by U.S. FDA, Health Canada, EMEA and ANVISA along with sponsor study and site qualification audits. Mr. O’Connor’s strong organizational, management and decision making skills contribute significantly to team effectiveness.