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My  experience focuses on facilitating clinical research between industry sponsors, potential investigators,  and divisions within both the University Hospital and Primary Childrens Hospital. My responsibilites include providing protocol and regulatory support required for activation and maintenance of investigator-initiated trials, ensuring investigator-initiated protocols contain quality research design ensuring data-integrity. I also ensure that the trial conduct is in compliance with GCP, ICH,  requirements of the Institutional Review Board (IRB) and all applicable regulations. My team consists of  research site monitors, an IND/IDE team and marketing professionals working to ensure h...

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