Opportunity knocks but once, and the SASInstitute Clinical Trials Programming Using SAS 9.4 credential is worth answering for — Prep4pass equips you for the A00-282 exam with verified answers, daily-checked content, and service that replies within about three hours, any day of the year.
SASInstitute A00-282 Exam Overview:
| Certification Vendor: | SAS Institute |
|---|---|
| Exam Name: | Clinical Trials Programming Using SAS 9.4 |
| Exam Number: | A00-282 |
| Certificate Validity Period: | 5 years |
| Exam Format: | Short-answer, Multiple choice |
| Available Languages: | English |
| Related Certifications: | SAS Certified Specialist: Base Programming Using SAS 9.4 SAS Certified Professional: Advanced Programming Using SAS 9.4 |
| Exam Duration: | 110 minutes |
| Real Exam Qty: | 60-70 |
| Exam Price: | $180 USD |
| Passing Score: | 68% |
| Recommended Training: | SAS Clinical Trials Programming Curriculum Foundations of Clinical Trials Programming |
| Exam Registration: | Pearson VUE Registration SAS Certification Portal |
| Sample Questions: | ![]() |
| 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:
| Section | Weight | Objectives |
|---|---|---|
| Topic 1: Macro Programming for Clinical Trials | 15% | - Debugging macros - Macro variables and parameters - Create and call macros |
| Topic 2: Clinical Trials Process | 5% | - Clinical trial lifecycle and protocol - Derive programming requirements from protocol and CRF |
| Topic 3: Manage Clinical Trials Data | 5% | - Access and explore clinical datasets - Clean, merge, and subset data - Use SQL and dictionary tables |
| Topic 4: Clinical Trials Data Structures | 10% | - CDISC standards: SDTM, ADaM - Define.xml and dataset specifications - Clinical domain structures |
| Topic 5: Transform or Summarize Clinical Trials Data | 15% | - Aggregation and transposition - Data step manipulation - Derive variables and study days |
| Topic 6: Validate Clinical Trial Data Reporting | 20% | - Use PROC COMPARE and log review - Validation principles - Programming validation techniques |
| Topic 7: Report Clinical Trials Results | 10% | - PROC REPORT and PROC PRINT - Produce tables, listings, and figures |
| Topic 8: Apply Statistical Procedures for Clinical Trials | 15% | - Basic statistical analysis for clinical data - PROC MEANS, FREQ, TABULATE |
| Topic 9: Regulatory Submissions | 5% | - Compliance for clinical data reporting - ICH and FDA guidelines |
SASInstitute Clinical Trials Programming Using SAS 9.4 Details Every Buyer Should Read
- Clinical Trials Data Structures (10%)
- Validate Clinical Trial Data Reporting (20%)
- Regulatory Submissions (5%)
SASInstitute Clinical Trials Programming Using SAS 9.4 Sample Questions:
The PROC COMPARE code below is intended to validate the results from a PROC FREQ.
Both the ProdFreqData and ValFreqData data sets contain 10 observations of the variable Frequency.
No other variables are present in these data sets.
proc compare base = ProdFreqData
comp = ValFreqData
out = FreqDiffs
outbase outcomp outdif outnoeq
method = exact
noprint;
run;
After successfully executing this PROC COMPARE step, what is a possible reason for the FreqDiffs file to contain 30 records?
- A. The internal values of Frequency are different in the base and comparison data sets.
- B. The variable types of Frequency are different in the base and comparison data sets.
- C. The formatted values of Frequency are different in the base and comparison data sets.
- D. The variable labels of Frequency are different in the base and comparison data sets.
Correct Answer: A 🗳️
The programmer runs a validation program of the SDTM DM domain which produces the following in the log in SAS:
What does the validator need to check?
- A. The sort order of both the production and validation datasets.
- B. The formatted data values for SEX and AGE.
- C. The internal data values for SEX and AGE.
- D. The labels of both the production and validation datasets.
Correct Answer: C 🗳️
Which validation technique involves two programmers writing separate programs to produce the same output, then comparing the result?
- A. Peer Review
- B. Independent Programming
- C. Peer Matching
- D. Identical Programming
Correct Answer: B 🗳️
Which OPTION displays all SAS language statements generated during macro execution?
- A. MSTORED
- B. MLOGIC
- C. MPRINT
- D. MRECALL
Correct Answer: C 🗳️
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:
- A. a clinical trial plan
- B. a data management plan
- C. a protocol
- D. a statistical analysis plan
Correct Answer: C 🗳️





