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The Associate Clinical Research Coordinator is responsible for the coordination of clinical research protocols. Activities include, but are not limited to: protocol feasibility, subject recruitment, eligibility assessment, informed consent, study-specific procedures, data collection, case report form maintenance, protocol compliance, drug supply inventory, and interactions with physicians, clinical research associates, patients and others. The Associate Clinical Research Coordinator promotes Good Clinical Practice in the conduct of clinical investigations by possessing an in-depth knowledge of FDA regulations, human subject protection, and research regulation requirements.