The Association of Clinical Research Professionals

Understanding Clinical Trial Protocols: Key Considerations for Effective Development and Feasibility Review

Pricing With Contact Hours

Member: $22.50 | Nonmember: $149

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This course is approved for 1.5 ACRP contact hours. Accreditation Details

This course will be accessible for up to one year from the date of purchase.


Pricing Without Contact Hours

Member: $0 | Nonmember: N/A

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This eLearning course will be accessible for up to one year from the date of purchase.


Course Description

Improve your knowledge and skills in study protocol design and review.

The protocol is the heart of every clinical trial. It is the document that drives the content of the other essential documents in a clinical trial, from the informed consent form to case report forms and, ultimately, data collection and analysis to support or deny product approvals. Therefore, it is essential that all clinical research professionals fully understand protocol to effectively execute them.

This interactive eLearning course covers the anatomy of a protocol, hypothesis development, study design, subject safety and data integrity risk considerations, protocol feasibility and protocol amendments.

Learning Objectives

  • Describe how quality protocols are developed
  • Define the different study models and requirements for protocol authoring
  • Review protocols to ensure feasibility and compliance
  • Communicate the feasibility of a study

Audience

Clinical research professionals who develop, review, and/or execute clinical protocols

Bring this Program to Your Team — With an eLearning Site License, your team will have access to this and 20+ more training programs covering everything from the “essentials” of clinical research to specialized topics. Delivered on our platform or for use in your learning management system.
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