Mr. Popowicz has over 15 years of experience in the clinical research industry including five (5) years conducting medical device clinical research.  Mr. Popowicz has worked within sponsor organizations ranging from the top ten (10) device manufacturers to small, startup organizations focused on commercializing novel medical technologies.  In his current role, Mr. Popowicz provides clinical operational support to device organizations looking for approval or clearance of their devices and has developed multiple IDE trials, contributed to 510(k) submissions and supported de Novo trials. Mr. Popowicz has provided operational oversight in the areas of therapeutic strategic planning, literature searches, protocol development, enrollment modeling, site identification and feasibility, patient recruitment, trial management, publication development, and clinical evaluation reports. Mr. Popowicz has conducted over 20 presentations at industry conferences and publishes on topics to assist the device industry to increase their clinical operations efficiency.