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SASInstitute A00-281 Exam Overview:
| Certification Vendor: | SAS Institute |
|---|---|
| Exam Name: | SAS Certified Clinical Trials Programmer Using SAS 9 Accelerated Version |
| Exam Number: | A00-281 |
| Certificate Validity Period: | Valid for life (no expiration) |
| Exam Duration: | 110 minutes |
| Real Exam Qty: | 65-70 |
| Available Languages: | English |
| Passing Score: | 70% |
| Exam Format: | Short Answer, Multiple Choice |
| Exam Price: | $180 USD |
| Related Certifications: | SAS Certified Professional: Clinical Trials Programming Using SAS 9.4 (A00-282) SAS Certified Clinical Trials Programmer Using SAS 9 (A00-280) |
| Recommended Training: | SAS Programming for Clinical Trials Clinical Trials Programming Curriculum |
| Exam Registration: | Pearson VUE Registration SAS Certification Portal |
| Sample Questions: | SASInstitute A00-281 Sample Questions |
| Exam Way: | Online proctored or onsite testing at Pearson VUE centers |
| Pre Condition: | Must hold SAS Certified Base Programming Specialist (A00-211/A00-231) or Advanced Programming Professional; recommended 6+ months clinical trials programming experience |
| Official Syllabus URL: | https://www.sas.com/en_us/certification/credentials/foundation-tools/clinical-trials-programmer/clinical-trials-programming-accelerated-exam.html |
Duration, language, and format of Clinical Trials Programming Using SAS 9 Accelerated Version (A00-281) Exam
Format: Multiple choices, multiple answers
- Length of Examination: 2 hours
- Passing score: 70%
- Number of questions: 70-75
- Language: English
Here are the solution for the Clinical Trials Programming Using SAS 9 Accelerated Version (A00-281) Exam
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SASInstitute A00-281 Exam Syllabus Topics:
| Section | Weight | Objectives |
|---|---|---|
| Clinical Trials Data Structures | 10% | - CDISC standards: SDTM, ADaM - Types of clinical trial datasets - Annotated CRF and define.xml |
| 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% | - PROC TTEST, FREQ, MEANS, UNIVARIATE - Descriptive statistics - Generate analysis outputs |
| Transform or Summarize Clinical Trials Data | 15% | - Subset, merge, and restructure datasets - Derive analysis variables - Apply LOCF/BOCF techniques |
| Manage Clinical Trials Data | 5% | - Import/export data files - Handle missing data - Data cleaning and manipulation |
| Report Clinical Trials Results | 10% | - ODS statements for TLFs - PROC REPORT, TABULATE, PRINT - Format outputs for regulatory submission |
| Validate Clinical Trial Data Reporting | 25% | - Review SAS log for errors/warnings - Use PROC COMPARE for validation - Verify consistency of tables/listings/figures |
| Macro Programming for Clinical Trials | 15% | - Write reusable macro programs - Debug macro logic - Create and use macro variables |
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