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Duration, language, and format of Clinical Trials Programming Using SAS 9 Accelerated Version (A00-281) Exam
Format: Multiple choices, multiple answers
- Language: English
- Number of questions: 70-75
- Passing score: 70%
- Length of Examination: 2 hours
What is Clinical Trials Programming Using SAS 9 Accelerated Version (A00-281) Exam
This exam validates the candidate's ability for the clinical trial process, access, management and transformation of clinical trial data, statistical procedures and macroprogramming, communication of clinical trial results and validation. clinical trial data reports.
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Here is a procedure to register for the Clinical Trials Programming Using SAS 9 Accelerated Version (A00-281) Exam
In order to apply for the Clinical Trials Programming Using SAS 9 Accelerated Version (A00-281), You have to follow these steps
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- Step 3: Search for SAS Business Analytics Administration (A00-250) Exam Certifications Exam
- Step 4: Select Date, time and confirm with payment method
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SASInstitute A00-281 Exam Syllabus Topics:
| Section | Weight | Objectives |
|---|---|---|
| Validate Clinical Trial Data Reporting | 25% | - Review SAS log for errors/warnings - Use PROC COMPARE for validation - Verify consistency of tables/listings/figures |
| Manage Clinical Trials Data | 5% | - Data cleaning and manipulation - Import/export data files - Handle missing data |
| Clinical Trials Process | 5% | - Interpret Statistical Analysis Plan (SAP) - Clinical research phases and key roles - Regulatory requirements: GCP, ICH, 21 CFR Part 11 |
| Statistical Procedures for Clinical Trials | 15% | - Generate analysis outputs - PROC TTEST, FREQ, MEANS, UNIVARIATE - Descriptive statistics |
| Transform or Summarize Clinical Trials Data | 15% | - Subset, merge, and restructure datasets - Derive analysis variables - Apply LOCF/BOCF techniques |
| Clinical Trials Data Structures | 10% | - Annotated CRF and define.xml - Types of clinical trial datasets - CDISC standards: SDTM, ADaM |
| Report Clinical Trials Results | 10% | - ODS statements for TLFs - PROC REPORT, TABULATE, PRINT - Format outputs for regulatory submission |
| Macro Programming for Clinical Trials | 15% | - Create and use macro variables - Debug macro logic - Write reusable macro programs |
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