The series of three courses provides foundational knowledge of clinical research operations. The courses introduce the primary types and phases of clinical trials and detail what it takes to conduct efficient and effective research. They define the key roles of research and administrative personnel and outline organizational structures, operational budgets, clinical trial agreements, and third-party vendors. The courses provide the learner with fundamental knowledge of regulatory affairs, including discussions of informed consent, institutional review boards, investigator site files, regulatory matrixes, and statements of investigator.
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Organizational Subscription Price: Available for $675 per year/per site as a subscription add-on for government and non-profit organizations; $750 per year/per site as a subscription add-on for for-profit organizations.
