Etienne Hinton

TMF Systems Specialist @ Duke Clinical Research Institute

An experienced professional with over 15 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.”

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