SAS Clinical Training and Placement Program by Showtheropes


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For full curriculum and batch details contact or call us at +1-443-687-9600
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Course Details:

In this course, you will learn basics and advanced SAS concepts to read and manipulate clinical data. Using the clinical features and basic concepts of clinical trials, this course shows how to import ADAM, CDISC or other standards for domain structure and contents into the metadata, build clinical domain target table metadata from those standards, create jobs to load clinical domains, to validate the structure and content of the clinical domains based on the standards, and to generate CDISC standard define.xml files describing the domain tables for clinical submissions.

Training type: Online
Duration: 4-5 Weeks
Batch Timings: Morning, Evening and Weekend batches available

Who should attend?
Bioinformatics or Life Science Graduates
Job aspirants with basic understanding of clinical concepts or statistics
SAS Clinical Data Integration organizes, standardizes and manages clinical research data and metadata. It provides the foundation you need to ensure standard, trusted clinical data to support strategic analyses, such as cross-study and advanced safety analysis. With SAS, you can gain both speed and efficiency by automating repeatable clinical data integration tasks.

Class size is limited?sign up for this course today!

What you?ll learn?
BASE SAS and Advance SAS:
Basic SAS Concepts
Referencing files, setting Options, Editing and debugging SAS Programs
Creating List Reports and Enhanced List and summary reports
Creating SAS data sets from raw data
Understanding DATA step processing
Creating and applying user defined formats
Producing descriptive Statistics
Creating and managing variables
Reading SAS Data sets
Combining SAS data sets
Transferring Data with SAS functions
Generating Data with DO loops and processing variables with Array
Reading Raw Data in fixed fields
Advanced Base/SAS: Macros and Proc Sql

Clinical Programming
Explanation of organizational aspects of the Biometrics department
Basic concepts of Clinical trials
Phase ? I, Phase ? II, Phase ? III, Phase ? IV
Clinical trial glossary ? Demystified
Explanation of the Clinical trial process
Protocol development
CRF Design and development, Data Management plan
Edit check specifications document, Edit check programming
Data querying, Paper CRF and E-CRF studies
Database programming and basic understanding of EDC studies
Annotated CRF?s
Data Querying
Lab data handling ? procedures and pitfalls
Patient Profiles, Database Lock
CDISC SDTM 3.1.2 and ADAM 1.2 Implementation
How to generate Tables, Listing and Figures

For full curriculum and batch details contact or call us at +1-443-687-9600
Visit us at

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