Summit: Clin Ops Foundations

Practical instruction for clinical research operations.


About these Courses

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.

Note: Summit: Operations and Logistics and Summit: Clinical Research Regulatory are available now. Summit: Welcome to Clinical Research will be released soon.

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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.

Language Availability: English

Suggested Audiences: Clinical Research Coordinators (CRCs), Contract Research Organizations (CROs), Faculty, Investigators, Regulatory Affairs Professionals, Research Administrators, Study Sites


Basic Courses

Summit: Clinical Research Regulatory
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Provides fundamental knowledge of clinical trial regulatory affairs.

doctor and businesswoman speaking
Summit: Operations and Logistics
New

Provides fundamental knowledge on how to conduct efficient and effective clinical research.

Adult Asian female doctor


FAQs

What courses are included in the Summit: Clin Ops Foundation series?

Summit: Welcome to Clinical Research (coming soon), Summit: Operations and Logistics, and Summit: Clinical Research Regulatory courses comprise the series.

Who should take the Summit: Clin Ops Foundation courses?

The series is specifically intended for those who are responsible for conducting clinical research. Intended audiences include clinical research coordinators (CRCs), contract research organizations (CROs), faculty, investigators, regulatory affairs professionals, research administrators, students, and study sites.

How long will the course take a learner to complete?

Each course can be completed in 30-40 minutes.

Are the courses in the series eligible for continuing medical education credits?

These courses do not currently have CE/CME credits available.