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| 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 Format: | Multiple Choice, Short Answer |
| Exam Price: | $180 USD |
| Exam Duration: | 110 minutes |
| Available Languages: | English |
| Passing Score: | 70% |
| Real Exam Qty: | 65-70 |
| Related Certifications: | SAS Certified Clinical Trials Programmer Using SAS 9 (A00-280) SAS Certified Professional: Clinical Trials Programming Using SAS 9.4 (A00-282) |
| Recommended Training: | SAS Programming for Clinical Trials Clinical Trials Programming Curriculum |
| Exam Registration: | Pearson VUE Registration SAS Certification Portal |
| 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 |
| Section | Weight | Objectives |
|---|---|---|
| Statistical Procedures for Clinical Trials | 15% | - Generate analysis outputs - Descriptive statistics - PROC TTEST, FREQ, MEANS, UNIVARIATE |
| Report Clinical Trials Results | 10% | - ODS statements for TLFs - Format outputs for regulatory submission - PROC REPORT, TABULATE, PRINT |
| Clinical Trials Data Structures | 10% | - Annotated CRF and define.xml - Types of clinical trial datasets - CDISC standards: SDTM, ADaM |
| Clinical Trials Process | 5% | - Clinical research phases and key roles - Regulatory requirements: GCP, ICH, 21 CFR Part 11 - Interpret Statistical Analysis Plan (SAP) |
| Transform or Summarize Clinical Trials Data | 15% | - Derive analysis variables - Apply LOCF/BOCF techniques - Subset, merge, and restructure datasets |
| Manage Clinical Trials Data | 5% | - Handle missing data - Data cleaning and manipulation - Import/export data files |
| Macro Programming for Clinical Trials | 15% | - Write reusable macro programs - Create and use macro variables - Debug macro logic |
| Validate Clinical Trial Data Reporting | 25% | - Use PROC COMPARE for validation - Verify consistency of tables/listings/figures - Review SAS log for errors/warnings |
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Currently, the A00-281 exam requires a passing score of 70% and carries a registration fee of $180 USD. SASInstitute can revise either figure, so confirm both on the official site before you schedule.
Because every step is built to save time. The A00-281 bank is carefully made — expert-verified answers across the SASInstitute SAS Certified Clinical Trials Programmer Using SAS 9 Accelerated Version objectives, organized for efficient study rather than endless reading. Delivery is instant upon payment, updates are free for 365 days and arrive by email automatically, and our customer service team is online 24 hours to give fast, precise replies whenever a question about the materials comes up. Efficiency is the design goal, from first click to exam day.
The SASInstitute SAS Certified Clinical Trials Programmer Using SAS 9 Accelerated Version blueprint is structured around these main domains:
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Per the latest exam information, the A00-281 exam includes 65-70 questions and allows 110 minutes minutes. Rehearsing under the same limit at home removes one more unknown from exam day.
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SASInstitute lists these prerequisites for the SASInstitute SAS Certified Clinical Trials Programmer Using SAS 9 Accelerated Version: Must hold SAS Certified Base Programming Specialist (A00-211/A00-231) or Advanced Programming Professional; recommended 6+ months clinical trials programming experience.
Confirm the current requirements on the official certification page before registering.
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Which statement assigns the current date to the character variable CURRDT?
Correct Answer: D 🗳️
You want 90% confidence limits for a binomial proportion from a one-way table with PROC FREQ. Which option must you add to the TABLES statement?
Correct Answer: A 🗳️
An action plan that describes what will be done in a drug study, how it will be conducted, and why each part of the study is necessary is called:
Correct Answer: B 🗳️
Which statement will produce report output that can be opened in Microsoft Word?
Correct Answer: C 🗳️
Identify the CDISC model with the following characteristics:
XML-based content and format standard
facilitates the archive and interchange of the metadata and data for clinical research
provides an accurate audit trail that is 21 CRF Part II compliant
Correct Answer: A 🗳️
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