Nicholas J. Meo, BA
Senior Clinical Research Coordinator

Nick Meo has more than 30 years of experience in the human and animal health pharmaceutical industry including research and development, clinical research, quality assurance and regulatory affairs.

Mr. Meo has worked for Sterling Drug, Rhone Merieux, Merial, and Velcera. He has coordinated activities required to conduct multiple-site laboratory and clinical studies, monitored veterinary clinical and non-clinical studies under FDA and EPA regulatory conditions (GLP and GCP) in a number of areas, and served as a study director for GLP human worker exposure studies. He also established a quality assurance system, developed a QA audit system at a manufacturing site (GMP), managed activities to rebuild a QA department at CRO (GLP), and administered SOPs.

His Regulatory Affairs experience includes protocol development, NADA submissions, interaction with FDA reviewers, and preparation of responses to site inspection citations and incomplete letters.
Mr. Meo’s strength in recruiting clinical research teams, training and supervising professional and technical staffs in clinical research procedures, quality assurance systems and government regulations makes him an essential member of AlcheraBio’s staff.