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(CRO), who in turn reports to the Vice President for Biomedical Graduate Education and Research. The Regulatory Coordinator collaborates closely with a wide range of stakeholders across the clinical
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protocol, the CRC2 is required to be the main point of contact for a patient in a clinical trial and must respond to inquiries from any patient within 24 hours. The CRC2 is instructed and required
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directly to the Director of the Clinical Research Organization (CRO), who in turn reports to the Vice President for Biomedical Graduate Education and Research. The Clinical Research Coordinator will have
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. Per the requirements of each clinical trial protocol, the CRC II is required to be the main point of contact for a patient in a clinical trial and must respond to inquiries from any patient within 24