Suzanne Lemoine

Suzanne M. Lemoine received her Bachelor and Master of Arts degrees in Sociology with an emphasis on research from the University of New Brunswick in Canada. Ms. Lemoine has over 11 years of experience in regulatory and clinical research. She has successfully managed the regulatory requirements from start-up to close out for numerous sponsor and principal investigator studies, created internal regulatory SOPs, and coordinated internal and sponsor monitoring of trials. She has a clear understanding of regulatory processes, procedures and policies, including GCP and local regulatory requirements.