President; Clinical Research Associate
CurrentProvide consulting services to Pharmaceutical and Medical Device Companies for phase 1 through phase 4 clinical trials; Investigator evaluation and selection; Site initiation and training; Onsite monitoring to ensure the rights and well being of human subjects are protected, that reported trial data are accurate, complete and verifiable by source documents and that trials are conducted within the currently approved protocol; Investigator site closure; To manage all Investigator site activities related to study sites assigned and according to all contracted services in compliance with current legislation, ICH CGP and appropriate company/Sponsor procedures and quality standards.