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Etienne Hinton

Duke Clinical Research Institute
Clinical Trial Coordinator I
An experienced professional with over 13 years of knowledge and experience in the CRO industry. During that spending time at both CROs and currently at an ARO. I contain a vast depth of experience and knowledge in drug safety, clinical affairs and site relationship management across multiple studies and in a variety of therapeutic areas. Working closely with internal teams as well as external sponsors, assuring adequate processes are developed and adhered to which increases safety for our patients. I enjoy developing processes for document management to assure proper documentation regarding documentation management I have developed a passion for clinical research and doing it right, there is an old saying “If it isn’t documented it didn’t happen”