Clinical SAS

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Clinical SAS

SAS is an extensive clinical trial data analysis in the Biopharmaceutical industries that generates a link between raw data and the analyzed data. Clinical trial aspects fused with knowledge of SAS commences to a challenging and worthwhile career that emphatically impacts & transforms medically dependent lives.


We have created a perfect curriculum, which trains you to be a clinical system analyst. Our curriculum includes the following:

Basic topics

  • Introduction to SAS
  • Basic Concepts (Files & Options)
  • Understanding Data Step Processing
  • Reading Raw Data into SAS
  • Reading Raw Data from External files
  • Reading Data from SAS Data Sets
  • Working with SAS Informatics & Formats
  • Working with SAS Functions
  • Creating Formats and Labels
  • Performing Conditional Processing
  • Combining SAS Data Sets
  • Performing Iterative Processing: Looping
  • Working with SAS Arrays
  • Summarizing the Data using Proc MEANS, PROC FREQ, PROC SUMMARY, etc.
  • Restructuring the data using Proc Transpose
  • Creating list and customized Reports using PROC REPORT

Advanced SAS topic

  • Performing Queries Using PROC SQL
  • Performing Advanced Queries Using PROC SQL
  • Combining Tables vertically, Using PROC SQL
  • Combining Tables horizontally, Using PROC SQL
  • Introducing Macro Variables
  • Macro Functions
  • Processing Macro Variables at Execution Time
  • Developing and Debugging Macros
  • How Does the Macro Processor Work

Domain related topics

  • Clinical Trials
  • Introduction to Clinical Trials
  • Regulatory Training
  • E3, E6, and E9 Guidelines
  • 21 CFR PART 11
  • Drug Development Process
  • Introduction to Statistical Programming
  • Statistical Programming
  • Statistical Programming Study Requirements

    • Study Documents

    • IT Requirements

  • Folder Structure
  • Understanding Protocol and Study Documents
  • Interpretation of SAP and Mock Shell

    • CDISC Introduction

  • SDTM Standards Theory discussion and Hands-on Programming on assigned study

    • Demographics (DM)

    • Subject Visits (SV)

    • Exposure (EX)

    • Adverse Events (AE)

    • Vital Signs (VS)

    • Concomitant Medication (CM)

    • Trial Designs

Other domains will involve, as per need and time availability

  • Creation of Table and Listings
  • ADAM Standards Theory + Hand-on Programming
  • CRF Annotation
  • Specification Creation for SDTM and ADAM
  • Mock Shell Annotation
  • Validation Techniques


The minimum eligibility criteria for the Professional course in Clinical SAS would include either of the following:

  • Any degree in Bioscience/Life Sciences such as Biochemistry, Microbiology, Genetics, Biotechnology, Botany, Zoology, etc.
  • Any degree in Medicine such as MBBS, BDS, BPT, BAMS, BHMS, BUMS, etc.
  • Any degree in Pharmacy / Pharmaceutical Sciences.
  • Any degree in Chemistry / Biostatistics / Bioinformatics.
  • Any degree in Nursing / Allied Health.
  • Students in their final year of graduation for the above courses are also eligible to apply.

If you are interested in Clinical SAS, we are happy to assist you through the process.

Download the course pdf for a detailed understanding before you begin your Clinical SAS Training with us!