SASInstitute A00-282 Exam : Clinical Trials Programming Using SAS 9.4

SASInstitute A00-282 exam
  • Exam Code: A00-282
  • Exam Name: Clinical Trials Programming Using SAS 9.4
  • Updated: Oct 21, 2026
  • Q & A: 144 Questions and Answers
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SASInstitute A00-282 Exam Overview:

Certification Vendor:SAS Institute
Exam Name:Clinical Trials Programming Using SAS 9.4
Exam Number:A00-282
Exam Price:$180 USD
Real Exam Qty:60-70
Certificate Validity Period:5 years
Available Languages:English
Exam Format:Multiple choice, Short-answer
Passing Score:68%
Related Certifications:SAS Certified Professional: Advanced Programming Using SAS 9.4
SAS Certified Specialist: Base Programming Using SAS 9.4
Exam Duration:110 minutes
Recommended Training:SAS Clinical Trials Programming Curriculum
Foundations of Clinical Trials Programming
Exam Registration:Pearson VUE Registration
SAS Certification Portal
Sample Questions:Free Download Pass A00-282 Exam Cram
Exam Way:Online proctored or onsite at Pearson VUE test centers
Pre Condition:Hold SAS Certified Specialist: Base Programming Using SAS 9.4 or SAS Certified Professional: Advanced Programming Using SAS 9.4; recommended 6+ months clinical trials programming experience
Official Syllabus URL:https://www.sas.com/en_us/certification/credentials/foundation-tools/clinical-trials-programming.html

SASInstitute A00-282 Exam Syllabus Topics:

SectionWeightObjectives
Validate Clinical Trial Data Reporting20%- Programming validation techniques
- Validation principles
- Use PROC COMPARE and log review
Transform or Summarize Clinical Trials Data15%- Derive variables and study days
- Data step manipulation
- Aggregation and transposition
Report Clinical Trials Results10%- PROC REPORT and PROC PRINT
- Produce tables, listings, and figures
Macro Programming for Clinical Trials15%- Macro variables and parameters
- Debugging macros
- Create and call macros
Regulatory Submissions5%- ICH and FDA guidelines
- Compliance for clinical data reporting
Clinical Trials Process5%- Clinical trial lifecycle and protocol
- Derive programming requirements from protocol and CRF
Apply Statistical Procedures for Clinical Trials15%- PROC MEANS, FREQ, TABULATE
- Basic statistical analysis for clinical data
Manage Clinical Trials Data5%- Use SQL and dictionary tables
- Access and explore clinical datasets
- Clean, merge, and subset data
Clinical Trials Data Structures10%- Define.xml and dataset specifications
- Clinical domain structures
- CDISC standards: SDTM, ADaM

SASInstitute Clinical Trials Programming Using SAS 9.4 Exam: Clean Tools, Honest Terms

The A00-282 exam is a SASInstitute certification exam validating the SASInstitute Clinical Trials Programming Using SAS 9.4 syllabus shown above. It belongs to these credential paths: SAS Certified Specialist: Base Programming Using SAS 9.4, SAS Certified Professional: Advanced Programming Using SAS 9.4. Candidates in 2026 start with VerifiedDumps's 144 practice questions, available as a printable PDF, a Windows Desktop Test Engine, and an Online Test Engine — three versions of the same materials.

The official SASInstitute Clinical Trials Programming Using SAS 9.4 outline defines 9 domains. The leading three are Clinical Trials Process (5%), Regulatory Submissions (5%), and Transform or Summarize Clinical Trials Data (15%). The full list is in the topics section above, and VerifiedDumps's 144 practice questions cover each one.

Hold SAS Certified Specialist: Base Programming Using SAS 9.4 or SAS Certified Professional: Advanced Programming Using SAS 9.4; recommended 6+ months clinical trials programming experience Since requirements change over time, confirm the latest on the official SASInstitute exam page before scheduling.

Three versions of the same study materials: a printable, expert-prepared PDF with free demo download and instant access; a Desktop Test Engine for Windows with customizable simulation and timed modes that works offline; and an Online Test Engine for any browser on Windows, Mac, Android, and iOS with test history and performance review. All 144 practice questions are identical across versions. Every purchase includes 365 days of free updates, a 50% renewal discount afterward, and unlimited computer installations.

The SASInstitute Clinical Trials Programming Using SAS 9.4 exam requires 68% to pass, and registration costs $180 USD. A failed attempt means paying the same fee again — a readiness check with the VerifiedDumps engines before booking is the cheaper option.

SASInstitute recommends these training resources for the SASInstitute Clinical Trials Programming Using SAS 9.4 exam:

Follow the training with steady self-testing — the 144 practice questions from VerifiedDumps help you apply theory and fill any gaps the training leaves.

The SASInstitute Clinical Trials Programming Using SAS 9.4 exam contains 60-70 to complete within 110 minutes. Timed simulation in the VerifiedDumps Desktop Test Engine teaches that rhythm before exam day does.

VerifiedDumps issues a full refund if you take the SASInstitute Clinical Trials Programming Using SAS 9.4 exam within 60 days of purchase and do not pass. The policy does not apply if the exam is taken within 3 days of purchase, if the exam was never actually taken, or to free materials or expired orders, and the candidate name must match the payer name. Submit a scan of your enrollment slip and the official Score Report PDF within 2 days of the exam; claims are processed within 7 days. Alternatively, exchange for two free exam products of equal value and keep your original update service. Orders arrive by email within 1 minute — contact support if nothing arrives within 2 hours.

Online proctored or onsite at Pearson VUE test centers Register for the SASInstitute Clinical Trials Programming Using SAS 9.4 exam through these official channels:

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SASInstitute Clinical Trials Programming Using SAS 9.4 Sample Questions:

Question #1

The following SAS program is submitted:
proc sort data=SASUSER.VISIT out=PSORT; by code descending date cost; run; Which statement is true regarding the submitted program?

  • A. The descending option applies to the variable CODE.
  • B. The descending option applies to the DATE and COST variables.
  • C. The variable CODE is sorted by ascending order.
  • D. The PSORT data set is stored in the SASUSER library.
Reveal Solution  Discussion  0

Correct Answer: C  🗳️

Question #2

Given the data set RAWBP that is sorted by SUBJECT TEST WEEK:

Baseline is defined as the week 0 value. Your colleague provides the following SAS program to calculate change from baseline:
data bp;
set rawbp;
by subject test week;
retain baseline;
if first.subject then baseline = value;
if week > 0 then change = value - baseline;
run;
What does the code calculate as the change from baseline for systolic blood pressure (SBP) at week 3?

  • A. 40
  • B. 30
  • C. -40
  • D. -30
Reveal Solution  Discussion  0

Correct Answer: B  🗳️

Question #3

The following question will ask you to provide a line of missing code. The following program is submitted to output observations from data set ONE that have more than one record per patient.

Please enter the line of code that will correctly complete the program. Note: Case is ignored. Do not add leading or trailing spaces to your answer.

  • A. BYSUBJID;
  • B. id;
    PTON run;
  • C. BYSUBJID;
    run;
  • D. BYSUBJID;
    BYSUBJID;
Reveal Solution  Discussion  0

Correct Answer: A  🗳️

Question #4

A SAS report procedure results in the log below.

What should you add to the PROC REPORT to address the blue note in this log?

  • A. Use DEFINE statements with the WIDTH= option set large enough to print all values for each variable
  • B. Specify COLWIDTH= option with a value large enough to print all values in the data
  • C. Use DEFINE statements where FLOW is specified for each numeric variable
  • D. Use a FORMAT statement with formats large enough to print all values for each numeric variable
Reveal Solution  Discussion  0

Correct Answer: D  🗳️

Question #5

Which statement describes an aspect of all Phase II clinical trials?

  • A. in vitro and in vivo experiments using wide-ranging doses of the drug
  • B. randomized controlled multicenter trials on large patient groups
  • C. designed to assess how well the drug works and further assess safety
  • D. designed to assess the pharmacovigilance, pharmacokinetics, and pharmacodynamics of a drug
Reveal Solution  Discussion  0

Correct Answer: C  🗳️

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