Anna C. Pavlick, MS, DO, Medical Director
Lisa R. Gaynes, Administrative Director
CTO personnel are available to both faculty and Industry sponsors to assist throughout the entire lifecycle of a protocol from inception to study closeout. We are the central point of contact who coordinate with Investigational Pharmacy, Laboratory, Nursing, OCT (study contract services), FDA, NCI and other collaborating Academic Institutions.
CTO services include ensuring regulatory compliance, complete IRB services; Protocol and Informed Consent Development; Quality Assurance; Safety monitoring and reporting ; Research Nursing; Data Management; Study Budgeting and Clinical Trials Education for faculty and staff. For Investigators wishing to participate in a Clinical Trial the first step is review by the PRMC (Protocol Review and Monitoring Committee).
Please contact Rachel Kennedy, the PRMC Coordinator who will assist you in initiating the process. Telephone: 212-263-4434 or email: firstname.lastname@example.org 
Click here for the Feasibility Committee  (Registered Members Only)