Jan J. Peterson MS, CCRA, RAC, MICR, ASQ CBA

Jan Peterson is a member of the ACRP Regulatory Affairs Committee, a contributing Item Writer for the Global CCRA® exam, a Senior Member of the American Society for Quality and a Certified Biomedical Auditor. Mr. Peterson has extensive experience in basic pharmacology and clinical research across several therapeutic areas. He has wide experience in trial management, advising on regulatory strategy, preparing regulatory submissions, monitoring, and quality assurance auditing for clinical trials in the US and internationally. He presently serves as a Project Director and Senior Regulatory Affairs Advisor for government funded and commercial clinical trials in ophthalmology, pediatrics and infectious diseases. He is responsible for regulatory oversight and compliance for multiple drug, biologic and device trials at Emmes, assists with internal quality reviews and staff training in ICH GCP, selected clinical specialties, and trial quality management. He has worked at Emmes, a CRO, for over 16 years and previously worked in university, industry and consultancy settings.