Talented Independent Senior Clinical Research Associate including a well-qualified background in clinical monitoring with a track record of success in varied clinical research environments. GCP certified and completion of a trainer led oncology course. Experienced in monitoring multiple sites and protocols, applying regulatory requirements such as GCP and ICH guidelines, conducting clinical site evaluations, site initiations, maintenance, and close-out visits. Effective team player, acting as a mentor to colleagues and a key resource to both colleagues and site staff.
Word, Excel, PowerPoint, Medidata Rave, Inform, OmniComm Trialmaster, Medidata CTMS, IMPACT
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