The Simplest Guide to Clinical Trials Data Analysis with SAS
The Simplest Guide to Clinical Trials Data Analysis with SAS, available at $99.99, has an average rating of 4.36, with 38 lectures, 7 quizzes, based on 1305 reviews, and has 5949 subscribers.
You will learn about Get introduced to the Life Science/ Pharmaceutical industry in simple, visual pictures Learn the fundamental concepts of Clinical Drug Development / Clinical Trials processes Understand the various Phases of Clinical Trials in the context of SAS programming Get introduced to the various clinical study documents like Protocol, Statistical Analysis Plan etc. Understand raw data and how it is collected, stored, analysed and reported Work hands-on with sample study data that you will import, prepare, restructure and visualize Generate an actual Clinical Study Reports from the derived data you will create See for yourself how SAS programming is an integral part of putting a drug into the market A guide to the SAS Certified Clinical Trials Programmer Using SAS®9 Certification Exam This course is ideal for individuals who are Anyone wanting to get into the Life Science / Pharmaceutical industry and looking to work in this field or Want to take up a job as a Clinical SAS Programmer in a Pharma company or a CRO (Contract Research Org.) or Want to just play with data using the SAS Programming concepts It is particularly useful for Anyone wanting to get into the Life Science / Pharmaceutical industry and looking to work in this field or Want to take up a job as a Clinical SAS Programmer in a Pharma company or a CRO (Contract Research Org.) or Want to just play with data using the SAS Programming concepts.
Enroll now: The Simplest Guide to Clinical Trials Data Analysis with SAS
Summary
Title: The Simplest Guide to Clinical Trials Data Analysis with SAS
Price: $99.99
Average Rating: 4.36
Number of Lectures: 38
Number of Quizzes: 7
Number of Published Lectures: 37
Number of Published Quizzes: 7
Number of Curriculum Items: 49
Number of Published Curriculum Objects: 48
Number of Practice Tests: 1
Number of Published Practice Tests: 1
Original Price: $199.99
Quality Status: approved
Status: Live
What You Will Learn
- Get introduced to the Life Science/ Pharmaceutical industry in simple, visual pictures
- Learn the fundamental concepts of Clinical Drug Development / Clinical Trials processes
- Understand the various Phases of Clinical Trials in the context of SAS programming
- Get introduced to the various clinical study documents like Protocol, Statistical Analysis Plan etc.
- Understand raw data and how it is collected, stored, analysed and reported
- Work hands-on with sample study data that you will import, prepare, restructure and visualize
- Generate an actual Clinical Study Reports from the derived data you will create
- See for yourself how SAS programming is an integral part of putting a drug into the market
- A guide to the SAS Certified Clinical Trials Programmer Using SAS®9 Certification Exam
Who Should Attend
- Anyone wanting to get into the Life Science / Pharmaceutical industry and looking to work in this field
- Want to take up a job as a Clinical SAS Programmer in a Pharma company or a CRO (Contract Research Org.)
- Want to just play with data using the SAS Programming concepts
Target Audiences
- Anyone wanting to get into the Life Science / Pharmaceutical industry and looking to work in this field
- Want to take up a job as a Clinical SAS Programmer in a Pharma company or a CRO (Contract Research Org.)
- Want to just play with data using the SAS Programming concepts
This course gives an introduction to the Pharmaceutical/ Life Science industry in a simple and visual style that is easy to understand. It shows how SAS is used as a tool to work with the vast amount of clinical data within this industry. The course takes you through an example clinical study sample data, and generate various Clinical Study Reports that are submitted to the FDA (in the US) or other regulatory authorities in other countries. You will not only hone your SAS programming skills but will also learn essential concepts needed to work in the Pharma industry in the areas of Biostatistics and Clinical Data Management.
After the introduction to the pharma industry and learning relevant concepts about Clinical Trials, the course takes you through a hands-on training exercise to build the very important and fundamental Clinical Study Report called the Demographics Table.
You will begin with a sample clinical study data in an Excel sheet, then you will import it into SAS, derive all necessary variables as shown in the mock table, and finally generate a clinical study report. All this will be done using guided SAS Programming steps with detailed explanations at every step of programming. At the end of this course, you will have learnt to work with Clinical Study Data, generate a real Clinical Study Report, and extend those steps to build other reports that constitute Clinical Trial submissions to the regulatory bodies.
Prerequisites: You will need basic SAS programming knowledge to work with code discussed in this course. You can take my course on SAS programming (“The Simplest Guide to SAS Programming”) available on Udemy.
A guide to the following SAS certification exam:
-
SAS Certified Clinical Trials Programmer Using SAS 9
Earn a Certificate
When you finish listening to all videos, assignments, quizzes and practice exams, you’ll earn a Certificate that you can share with prospective employers and your professional network.
Course Curriculum
Chapter 1: Introduction
Lecture 1: Course Overview
Lecture 2: Download the eBook and Course Slides
Lecture 3: Components of the Pharma/ Life Science Industry
Lecture 4: Phases of Clinical Trials
Lecture 5: Data and Reports in Clinical Trials
Lecture 6: Types of data in Clinical Trials
Lecture 7: Section Conclusion
Chapter 2: Get to know the Clinical Study Documents
Lecture 1: Get to know the Clinical Study Documents – Section Overview
Lecture 2: Study Documents – The Clinical Study Protocol
Lecture 3: The Informed Consent
Lecture 4: The Inclusion- Exclusion Criteria
Lecture 5: The Statistical Analysis Plan (SAP), mock shells, and Case Report Forms (CRFs)
Lecture 6: Get to know Clinical Study Documents – Section Conclusion
Chapter 3: Building the Clinical Study Reports (CSR)
Lecture 1: Building the CSRs – Section Overview
Lecture 2: SAS OnDemand Registration
Lecture 3: Logging-in to SAS after registration
Lecture 4: General SAS Programming Steps for building any CSRs
Lecture 5: Understanding the Demographics Case Report Form (CRF)
Lecture 6: Understanding the Demographics Table
Lecture 7: Planning to program the Demographics Table
Lecture 8: Importing raw Demographics data into SAS
Lecture 9: Deciding which PROCs to use
Lecture 10: Deriving the AGE variable
Lecture 11: Obtaining Summary Statistics for AGE
Lecture 12: Adding the 3rd Treatment Group using Explicit Output
Lecture 13: Deriving the SEX variable
Lecture 14: Obtaining Summary Statistics for SEX
Lecture 15: Concatenating the COUNT and PERCENT variables
Lecture 16: Deriving the RACE variable
Lecture 17: Obtaining Summary Statistics for RACE
Lecture 18: Stacking all 3 Summary Statistics together
Lecture 19: Fixing the precision points
Lecture 20: Transposing data
Lecture 21: Fixing the order of statistical parameters
Lecture 22: Building the final report
Lecture 23: Putting the final touches to the report
Lecture 24: Building the CSRs – Section Conclusion
Chapter 4: Capstone Project
Instructors
-
Aslam Khan, M.S, PMP, PgMP
M.S., PgMP, PMP, SAS Base and Adv. certified
Rating Distribution
- 1 stars: 12 votes
- 2 stars: 25 votes
- 3 stars: 183 votes
- 4 stars: 521 votes
- 5 stars: 564 votes
Frequently Asked Questions
How long do I have access to the course materials?
You can view and review the lecture materials indefinitely, like an on-demand channel.
Can I take my courses with me wherever I go?
Definitely! If you have an internet connection, courses on Udemy are available on any device at any time. If you don’t have an internet connection, some instructors also let their students download course lectures. That’s up to the instructor though, so make sure you get on their good side!
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