The Association of Clinical Research Professionals

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

IMPORTANT: This training program will not be available for purchase between December 1, 2019 and January 6, 2020 while we transition to an improved training platform. If you purchase this program prior to December 1, 2019, you must complete the course evaluation before December 31, 2019 to receive ACRP contact hours.

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

An essential course for all clinical research professionals involved in the design and/or feasibility assessment of clinical research protocols. This interactive eLearning course incorporates a high level overview of concepts and real-world scenarios you are likely to encounter when developing a protocol.

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

Competency Domains

This course builds competence in the following domains:

  • Clinical Trials Operations (GCPs)
  • Medicines Development and Regulation
  • Scientific Concepts and Research Design
  • Study and Site Management

Learn About Competency Domains for Clinical Research Professionals >>

Tools Provided

  • Testing a Hypothesis
  • Protocol Components Worksheet
  • Research Design Models
  • Feasibility Assessment Checklist
  • Case Study Guide

Audience

Clinical research professionals involved with protocol development and/or feasibility assessment.