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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 course builds practical skills for designing, analysing, and interpreting clinical trials confidently. Master setting objectives, defining endpoints, calculating sample sizes and power, planning interim analyses, managing multiplicity, and handling time-to-event data, hospitalisations, and sensitivity analyses for rigorous, transparent, publication-ready results.

Elevify advantages

Develop skills

  • Design heart failure trials by defining endpoints, estimands, and target population.
  • Calculate sample size and power using t-test formulas and sensitivity checks.
  • Plan interim analyses with information fractions, stopping rules, and DMC workflow.
  • Control multiplicity through hierarchical testing and SAP-compliant strategies.
  • Interpret trial results by linking HRs, CIs, and MCID to clinically relevant messages.

Suggested summary

Before starting, you can change the chapters and 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

I was just promoted to Intelligence Advisor for the Prison System, and the course from Elevify was crucial for me to be chosen.
EmersonPolice Investigator
The course was essential to meet my boss's and the company's expectations.
SilviaNurse
Very great course. Lots of rich information.
WiltonCivil Firefighter

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