Over 10 years of health care experience; worked in various hospital settings. Knowledgeable Clinical Research Associate with a drive to use said knowledge in research ethics review, performing and documenting pre-study site evaluations, regulatory document collection, interim monitoring, and study close-out visits. Diligent in performing studies aligned with good clinical practices, study-specific requirements, and clinical monitoring plans. In-depth knowledge of the importance of standard operating procedures, regulatory requirements, and quality standards.
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