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Clinical Trials Programming Using SAS 9 Accelerated Version (A00-281) Exam Reference
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SASInstitute A00-281 Exam Syllabus Topics:
| Section | Weight | Objectives |
|---|---|---|
| Manage Clinical Trials Data | 5% | - Apply clinical data management concepts - Import, access, and manage clinical trial data |
| Validate Clinical Trial Data Reporting | 20% | - Validate clinical trial outputs - Perform quality control programming |
| Report Clinical Trials Results | 10% | - Create clinical trial reports - Produce tables, listings, and reports |
| Transform or Summarize Clinical Trials Data | 15% | - Use SAS DATA step programming techniques - Create derived datasets and variables |
| Macro Programming for Clinical Trials | 15% | - Automate clinical programming tasks - Create and use SAS macros |
| Apply Statistical Procedures for Clinical Trials | 15% | - Use SAS statistical procedures - Analyze clinical trial data |
| Clinical Trials Programming Concepts | - Clinical trial programming standards and practices - CDISC standards and clinical data structures | |
| Regulatory Submissions | 5% | - Prepare data and documentation for regulatory submission |
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