Packt
The Simplest Guide™ to Clinical Data Analysis with SAS
Packt

The Simplest Guide™ to Clinical Data Analysis with SAS

Included with Coursera Plus

Gain insight into a topic and learn the fundamentals.
Beginner level

Recommended experience

3 hours to complete
3 weeks at 1 hour a week
Flexible schedule
Learn at your own pace
Gain insight into a topic and learn the fundamentals.
Beginner level

Recommended experience

3 hours to complete
3 weeks at 1 hour a week
Flexible schedule
Learn at your own pace

What you'll learn

  • Describe the fundamental concepts of clinical drug development and trials.

  • Identify and explain the various phases of clinical trials in the context of SAS programming.

  • Recognize and utilize various clinical study documents.

  • Collect, organize, and analyze data using SAS.

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Recently updated!

October 2024

Assessments

1 assignment

Taught in English

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There are 3 modules in this course

In this module, we will introduce the foundational aspects of the pharma/life sciences industry, focusing on the clinical trial process. We’ll explore industry components, phases of clinical trials, and the various data types and reports integral to clinical research.

What's included

6 videos1 reading

In this module, we will delve into the essential documents involved in clinical studies. We’ll examine the clinical study protocol, informed consent, inclusion-exclusion criteria, and key analytical documents like the SAP, mock shells, and CRFs.

What's included

6 videos

In this module, we will guide you through the creation of Clinical Study Reports using SAS. We’ll cover the basics of SAS registration, explore programming steps for CSRs, and focus on building demographic tables and deriving key variables such as AGE, SEX, and RACE.

What's included

24 videos1 assignment

Instructor

Packt - Course Instructors
Packt
371 Courses8,562 learners

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Packt

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