Geoffrey Schick is a clinical trials research and compliance expert with 15+ years experience in leadership positions for large, integrated healthcare delivery systems.  Geoffrey also has 10+ years experience in clinical research consulting while working for several firms and independently.  In his leadership roles, Geoffrey has successfully developed and implemented workflows that ensure strong research billing compliance, and developed centralized clinical research administration programs. Geoffrey is a frequent research billing compliance speaker at national clinical trial conferences, including MAGI, ACRP, SoCRA, and HCCA Compliance Institute.