SASInstitute A00-281 Exam : SAS Certified Clinical Trials Programmer Using SAS 9 Accelerated Version

  • Exam Code: A00-281
  • Exam Name: SAS Certified Clinical Trials Programmer Using SAS 9 Accelerated Version
  • Updated: Jun 02, 2026
  • Q & A: 99 Questions and Answers

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About SASInstitute A00-281 Exam Questions

SASInstitute A00-281 Exam Syllabus Topics:

TopicDetails
Topic 1
  • Use SAS procedures to obtain descriptive statistics for clinical trials data
  • Identify the classes of clinical trials data
Topic 2
  • Explain the principles of programming validation in the clinical trial industry
  • Apply regulatory requirements to exported SAS data sets
Topic 3
  • Describe the structure and purpose of the CDISC SDTM data model
  • Examine and explore clinical trials input data
Topic 4
  • Import and Export Clinical Trials Data
  • Validate Clinical Trial Data Reporting
Topic 5
  • Use ODS and global statements to produce and augment clinical trials reports
  • Describe the structure and purpose of the CDISC ADaM data model
Topic 6
  • Use PROC TTEST to obtain p-values for continuous data
  • Describe the contents and purpose of define.xml
Topic 7
  • Use PROC REPORT to produce tables and listings for clinical trials reports
  • Describe the clinical research process
Topic 8
  • Utilize the log file to validate clinical trial data reporting
  • Access DICTIONARY Tables using the SQL procedure
Topic 9
  • Apply 'observation carry forward' techniques to clinical trials data
  • Create output data sets from statistical procedures

Reference: https://www.sas.com/en_us/certification/credentials/foundation-tools/clinical-trials-programmer/clinical-trials-programming-accelerated-exam.html

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Here are the topics of Clinical Trials Programming Using SAS 9 Accelerated Version (A00-281) Exam

Candidates must know the exam topics before they start of preparation. Because it will really help them in hitting the core. Our Clinical Trials Programming Using SAS 9 Accelerated Version A00-281 exam dumps will include the following topics:

Clinical Trials Process

  • Automate programs by defining and calling macros.
  • Use system options to debug macros and display values of macro variables in the SAS log (MPRINT, SYMBOLGEN, MLOGIC, MACROGEN). Report Clinical Trials Results
  • Identify and Resolve data, syntax and logic errors.
  • Obtain counts of events in clinical trials. Apply Statistical Procedures for Clinical Trials
  • Use programming techniques to validate clinical trial data reporting (PROC COMPARE, MSGLEVEL).
  • Identify the classes of clinical trials data (demographic, lab, baseline, concomitant medication, etc.).
  • Calculate ‘change from baseline' results.
  • Create output data sets from statistical procedures. Macro Programming for Clinical Trials
  • Apply categorization and windowing techniques to clinical trials data.
  • Use ODS and global statements to produce and augment clinical trials reports. Validate Clinical Trial Data Reporting
  • Apply ‘observation carry forward' techniques to clinical trials data (LOCF, BOCF, WOCF).
  • Explain the principles of programming validation in the clinical trial industry.
  • Derive programming requirements from an SAP and an annotated Case Report Form.
  • Identify key CDISC principals and terms.
  • Create and use user-defined and automatic macro variables.
  • Use PROC TTEST to obtain p-values for continuous data (one-sample, paired and two-sample t-tests).
  • Describe the structure and purpose of the CDISC ADaM data model.
  • Transpose SAS data sets.
  • Describe the clinical research process (phases, key roles, key organizations).
  • Describe the contents and purpose of define.xml. Import and Export Clinical Trials Data
  • Use PROC REPORT to produce tables and listings for clinical trials reports.
  • Describe regulatory requirements (principles of 21 CFR Part 11, International Conference on Harmonization, Good Clinical Practices). Clinical Trials Data Structures
  • Describe the structure and purpose of the CDISC SDTM data model.
  • Interpret a Statistical Analysis Plan.
  • Examine and explore clinical trials input data (find outliers, missing vs. zero values, etc). Transform Clinical Trials Data
  • Use PROC FREQ to obtain p-values for categorical data (2x2 and NxP test for association).
  • Apply regulatory requirements to exported SAS data sets (SAS V5 requirements). Manage Clinical Trials Data
  • Use SAS procedures to obtain descriptive statistics for clinical trials data (FREQ, UNIVARIATE, MEANS, SUMMARY).
  • Access DICTIONARY Tables using the SQL procedure.
  • Utilize the log file to validate clinical trial data reporting.

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How can you study for the Clinical Trials Programming Using SAS 9 Accelerated Version (A00-281) Certification Exam

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Clinical Trials Programming Using SAS 9 Accelerated Version (A00-281): Get our quick guide if you don't have time to read all the page

The SAS Certified Clinical Foundation Accelerated Version certification is considered the reference point for knowledge, skills and proven ability to identify classes of clinical study data (demographic, laboratory and reference data. The SAS Clinical Foundation Accelerated Version certification is a certification a very important passage in the A00-281 program of the SAS Institute certification hierarchy for the planning of clinical studies using the credentials of the accelerated version of SAS 9 confirms that you have a solid knowledge base on the fundamentals of computer science and to support the accelerated version SAS Certified Clinical Foundation For this, it is necessary to eliminate SAS Institute A00-281 Planning of clinical studies using the accelerated version of SAS 9. Exam A00-281 (Planning of clinical studies with version a This SAS 9 Accelerated is one of the fundamental computer exams that must be passed for obtaining certification for the accelerated version of the SAS Certified Clinical Foundation.

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