Description
Clinical trials vary widely in design. It is important to understand the design of a trial to be able to effectively review protocols, complete ethics committee submissions, write patient information sheets as well as to design clinical trials.
This course will give delegates:
- the different trial designs
- the considerations needed when designing a trial
- a structure for effective protocol review
- This course is suitable for anyone who is involved in clinical trials.
Who is the course suitable for?
The course is suitable for
- CRAs
- CTAs
- Study Nurses
- Investigators
- Data Managers
- Project Managers
- Clinical Trial Coordinators
- Medical Advisers
Course Content
Trial designs
- Parallel
- Cross-over
- Non-comparative
- Challenges and limitations
- Bias
Types of trial
- Objectives
- Difference/superiority trials
- Equivalence
- Non-inferiority
Endpoints
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