Bryan Nowak

Bryan Nowak is an experienced professional in document management and regulatory affairs, with a career spanning over two decades. Notable positions include serving as a Study Document Specialist and Regulatory Document Specialist at Merck & Company, where responsibilities included managing regulatory files and Informed Consent Forms for clinical trials. At ICON plc, Bryan Nowak currently holds the title of Associate Director TMF Services/Document Management, overseeing the setup and maintenance of Trial Master Files. Prior roles at organizations such as Pharmanet Development Group and PRA Health Sciences highlight expertise in regulatory submissions, team management, and compliance. Bryan Nowak holds a Master of Science in Management and several undergraduate degrees in Business Administration from Gwynedd-Mercy University.