Biostatistics and Clinical Research

Build a strong foundation in biostatistics for clinical drug research and trial evaluation.

Core Topics

2-3

Days

100%

Practical Focus

∞

Evidence Quality

About This Curriculum

Build a strong foundation in biostatistics for clinical drug research. This curriculum is designed for professionals who want to understand, design, and evaluate clinical trials with confidence.

Participants develop practical, real-world statistical skills and the ability to communicate results clearly across teams for regulatory and development settings.

Duration

Applied statistics labs with hands-on practice

Format

Interactive sessions with trial design and statistical analysis

Participants

Clinical research and regulatory affairs professionals

Outcomes

Statistical competence and evidence-based decision making

Key highlights

What makes this curriculum unique

Defining research questions and trial objectives

Trial designs: superiority and non-inferiority

Randomisation, blinding, and handling drop-outs

Relative risk, odds ratio, rate difference, and confidence intervals

Kaplan-Meier curves, logrank tests, and hazard ratios

Statistical testing, p-values, and sample size calculations

Managing multiple endpoints and non-inferiority margins

Stepwise non-inferiority to superiority testing

Strengthen evidence quality

Enable teams to design, interpret, and communicate clinical trial results with confidence.