Clinical Trials Course

Preview certificate

What will I learn?

Improve your skills in clinical trials with our full course made for healthcare workers. Learn about ethics, like getting agreement from people taking part and keeping their information safe. Also, learn how to plan trials and write up trial plans. Understand the different stages of trials, how to collect information, and how to look at the numbers. Learn how to deal with problems like side effects and people leaving the trial. Our short, good modules with lots of practice will help you get the skills you need to do well in clinical research.

Apoia's Unique Features

Online course with lifetime access
Certificate aligned with educational standards
Printable PDF summaries
Online support always available
Select and arrange the chapters you wish to study
Customize your course workload
Instant feedback on practical activities
Study anytime, no internet connection required

Develop skills

Enhance the growth of the practical skills listed below

Know the ethical rules: Make sure people agree to take part and that their information is protected.

Plan good trials: Make effective randomised controlled trials.

Write trial plans: Create complete clinical trial plans.

Look at information: Use statistics and computer programs.

Deal with problems: Handle side effects and keep the trial running properly.

Suggested summary

Workload: between 4 and 360 hours

Before starting, you can modify the chapters and the workload.

  • Select which chapter to commence with
  • Add or remove chapters
  • Increase or decrease the course workload

Examples of chapters you can include

You’ll be able to generate additional chapters similar to the examples below

This is a free course focused on personal and professional growth. It does not equate to a technical, undergraduate, or postgraduate qualification, but offers practical and relevant knowledge for your professional journey.