The Association of Clinical Research Professionals

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

This interactive training program incorporates a high-level overview of concepts and real-world scenarios you are likely to encounter when developing a protocol.

This is an essential program for all clinical research professionals involved in the design and/or feasibility assessment of clinical research protocols.

Participants get access to a variety of tools, including:

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

Upon completion of this training program, participants should be able to:

  • 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.

This course helps clinical researchers involved with protocol development and/or feasibility assessment build competency in Clinical Trials Operations (GCPs), Medicines Development and Regulation, Scientific Concepts and Research Design, and Study and Site Management. Explore Competencies >

Approved for 1.5 ACRP Contact Hours | Available 1 Year from Enrollment Date