The role of Clinical Research Coordinator II involves overseeing clinical trial protocols, which includes tasks such as patient identification, screening, and enrollment processes. Additionally, this position entails direct patient care responsibilities, such as conducting blood draws, administering medications, and performing physical assessments, all while adhering to stringent regulatory standards. Applicants should possess over 3 years of experience in clinical research coordination and have the legal right to work in the United States. This position demands a keen eye for detail, outstanding communication abilities, and proficiency in managing several study protocols at once.
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