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Clinical Trial Statistics Course

Clinical Trial Statistics Course
from 4 to 360h flexible workload
valid certificate in your country

What will I learn?

This Clinical Trial Statistics Course equips you with practical skills to design, analyse, and interpret modern trials confidently. You will learn to establish clear objectives, define endpoints, compute sample size and power, schedule interim analyses, manage multiplicity, and address time-to-event outcomes, hospitalisations, and sensitivity analyses, ensuring your results are rigorous, transparent, and ready for publication.

Elevify advantages

Develop skills

  • Design heart failure trials: define endpoints, estimands, and target population.
  • Calculate sample size and power: apply t-test formulas and run sensitivity checks.
  • Plan interim analyses: set information fractions, stopping rules, and DMC workflow.
  • Control multiplicity: build hierarchical testing and document SAP-compliant strategies.
  • Interpret trial results: link HRs, CIs, and MCID to clear, clinically relevant messages.

Suggested summary

Before starting, you can change the chapters and the workload. Choose which chapter to start with. Add or remove chapters. Increase or decrease the course workload.
Workload: between 4 and 360 hours

What our students say

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EmersonPolice Investigator
The course was essential to meet the expectations of my boss and the company where I work.
SilviaNurse
Very great course. Lots of rich information.
WiltonCivil Firefighter

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