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 >