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Clinical Trial Statistics Course

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

What will I learn?

Acquire practical skills in designing, analysing, and interpreting clinical trials confidently. Master setting objectives, defining endpoints, computing sample sizes and power, planning interim looks, managing multiplicity, and analysing time-to-event data, hospitalisations, and sensitivity checks 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 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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The course was essential to meet the expectations of my boss and the company I work for.
SilviaNurse
Very great course. Lots of rich information.
WiltonCivil Firefighter

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