Clinical Research Associate
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Certified Clinical Research Associate with 2+ years of progressive experience in monitoring, site management, and regulatory compliance across diverse clinical environments. Proven track record of ensuring ICH-GCP, FDA, and local regulatory adherence while managing cardiovascular-focused and interdisciplinary trials. Skilled in remote collaboration, optimizing clinical operations using CTMS, EDC, and TMF systems.
Adept at improving trial delivery timelines and site performance through data-driven insights and cross-functional teamwork.
