SAS Clinical

Duration of       Hours 


Duration time may vary depends on course progress


SAS Clinical


provides the foundation you need to ensure standard, trusted clinical data to support strategic analyses, such as cross-study and advanced safety analysis SAS is widely used in clinical trial data analysis in pharmaceutical, biotech and clinical research companies. The SAS Global Certification program includes credentials that validate SAS skills in Programming, Analytics, Data Science, Administration, Data Management and Enterprise Business Intelligence.

Training Objectives of SAS CLINICAL:

Clinical trials methodologies

Performing statistical analysis and macro programming

Creating clinical trials graphs



Course Content


  •  Clinical research Process

  •  Data management Advanced

  •  Study Protocol Briefing and Extraction

  •  CRF design

  •  Database spec and Edit check preparation


  •  Administration

  •  PL/SQL basics

  •  Users, Roles, Assigning user roles, User specific screens management

  •  PSUB, batch jobs administration

  •  Glib Admin – Reference code lists

  •  Study Plan

  •  Design – Create and maintain – Studies, Investigators, Sites, Visits and patients

  •  Definitions

  •  DVGs

  •  Questions, Question Groups

  •  DCM

  •  DCI

  •  Validation programming

  •  Data extract views administration

  •  Test a study

  •  Test Data entry

  •  Conduct

  •  Data validation (Discrepancy management)

  •  Execute – Batch jobs, Procedures, DCF forms.

  •  Data Extract

  •  Batch data, Out of study data load

  •  Conduct security

  •  Patient lock and freeze, study lock and freeze

  •  Mass changes

  •  Data entry (first pass, second pass), update, browse and key changes.

  •  Lab data load and administration

  •  RDC Administration

  •  RDC Workflow and discrepancy management


  •  Integration OC AE term, MT term and combed terms with TMS and medical coding and review

  •  TMS dictionary and maintenance

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