What is it? Why is it important?

A statistician uses statistics with the aim to help researchers in the interpretation of their data.

 

Tasks may include support:

 

  • After data collection:
    • Validate the data to ensure there are no obvious mistakes (e.g. dates = 2032, unrealistic vital signs such as body temperature = 85°C)
    • Prepare the data for analysis (e.g. derive new variables, such as BMI calculations based on weight and height)
    • Analyse the data (e.g. based on specifications given in a study protocol)
    • Present the statistical results by writing a statistical report
    • Assist in the publication of the study (e.g. scientific publications, abstract, posters)

What do I need to do?

As a SP-INV request the assistance of a statistician as early as possible (e.g. during the concept phase of your study).

 

A statistician can:

  • Assist in study planning, such as the selection of an appropriate study design, set-up of the study’s randomisation procedures, select the appropriate statistical methods
  • Assist in writing the statistical section of the study protocol
  • Perform the statistical analysis during study conduct (e.g. interim analysis) and upon study termination
  • Write the statistical report
  • Assist in the presentation of study results (e.g. publications, posters)

 

As a SP-INV, ensure the study statistician has the appropriate education and training needed to manage the statistical aspects of your study. 

 

Typically, a statistician has no education in medicine. Good communication and a close collaboration is therefore the key to success.

Where can I get help?

Your local CTU can support you with experienced staff regarding this topic

References

ICH Topic E9 statistical Principles for Clinical Trials – see in particular

  • 1.1. Background and Purpose
Abbreviations
  • CTU – Clinical Trials Unit
  • ICH – International Council for Harmonisation
  • BMI – Body Mass Index
  • SP-INV – Sponsor Investigator
Basic ↦ Statistics ↦ Statistics ↦ Statistician Role
Study
Basic

Provides some background knowledge and basic definitions

Basic Monitoring
Basic Drug or Device
Concept

Starts with a study idea

Ends after having assessed and evaluated study feasibility

Concept Drug or Device
Development

Starts with confidence that the study is feasible

Ends after having received ethics and regulatory approval

Development Drug or Device
Set-Up

Starts with ethics and regulatory approval

Ends after successful study initiation

Set-Up Ethics and Laws
Set-Up Quality and Risk
Set-Up Drug or Device
Conduct

Starts with participant recruitment

Ends after the last participant has completed the last study visit

Conduct Drug or Device
Completion

Starts with last study visit completed

Ends after study publication and archiving

Completion Statistics
Completion Drug or Device
Current Path (click to copy): Basic ↦ Statistics ↦ Statistics ↦ Statistician Role

Please note: the Easy-GCS tool is currently under construction.