Welcome to R for clinical study reports and submission book club! Let's prepare you for your future job in clinical data science.

Clinical study reports are essential parts of clinical trial development. A CSR is an “integrated” full scientific report of an individual clinical trial. The International Council for Harmonisation Efficiency 3, or ICH E3, structure and content of clinical study reports provides guidance to assist sponsors in the development of a CSR.

In this book club, you will learn how to use R to prepare a CSR and how to submit it to regulatory agencies by reading R for Clinical Study Reports and Submission. At each weekly meeting, we'll review two chapters from the linked book and work together on a slide deck of resources to reference after reading.

Visit the associated GitHub repository to explore more!