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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
Certificate Validity Period:5 years
Real Exam Qty:60-70
Exam Duration:110 minutes
Available Languages:English
Passing Score:68%
Exam Format:Multiple choice, Short-answer
Related Certifications:SAS Certified Professional: Advanced Programming Using SAS 9.4
SAS Certified Specialist: Base Programming Using SAS 9.4
Recommended Training:Foundations of Clinical Trials Programming
SAS Clinical Trials Programming Curriculum
Exam Registration:Pearson VUE Registration
SAS Certification Portal
Sample Questions:SASInstitute A00-282 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:

SectionWeightObjectives
Manage Clinical Trials Data5%- Clean, merge, and subset data
- Use SQL and dictionary tables
- Access and explore clinical datasets
Report Clinical Trials Results10%- PROC REPORT and PROC PRINT
- Produce tables, listings, and figures
Regulatory Submissions5%- ICH and FDA guidelines
- Compliance for clinical data reporting
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
Clinical Trials Data Structures10%- Clinical domain structures
- Define.xml and dataset specifications
- CDISC standards: SDTM, ADaM
Apply Statistical Procedures for Clinical Trials15%- Basic statistical analysis for clinical data
- PROC MEANS, FREQ, TABULATE
Clinical Trials Process5%- Derive programming requirements from protocol and CRF
- Clinical trial lifecycle and protocol
Macro Programming for Clinical Trials15%- Debugging macros
- Create and call macros
- Macro variables and parameters

SASInstitute Clinical Trials Programming Using SAS 9.4 Sample Questions:

Question 1

Given the file sites.csv:

Which option would you need to add to the INFILE statement to clear the notes from this log?

A. start=2
B. missover
C. firstobs=2
D. lrecl=2


Question 2

What is an international ethical and scientific quality standard for designing, conducting, recording and reporting trials that involve the participation of human subjects

A. 21 CFR Part 11
B. WHODrug
C. Good Clinical Practices
D. MedDRA


Question 3

What is the primary purpose of programming validation?

A. Document all specifications pertaining to programmed output and ensure all were reviewed during the programming process.
B. Ensure that the output from both the original program and the validation program match.
C. Efficiently ensure any logic errors are discovered early in the programming process.
D. Justify the means used to accomplish the outcome of a program and ensure its accurate representation of the original data.


Question 4

Which program will report all created output objects in the log?

A. ods trace on; proc ttest data=WORK.DATA1; class TREAT; var RESULTS; run;
B. ods trace log; proc ttest data=WORK.DATA1; class TREAT; var RESULTS; run;
C. proc ttest data=WORK.DATA1 ods=trace; class TREAT; var RESULTS; run;
D. ods trace=log; proc ttest data=WORK.DATA1; class TREAT; var RESULTS; run;


Question 5

A subject reports a medication started in March of 2007 but cannot recall the day number.
What is the value stored in the SDTM domain CM.CMSTDTC variable?

A. 2007-03
B. 00MAR2007
C. 2007 03
D. MAR2007


Solutions:

Question 1
Answer: C
Question 2
Answer: C
Question 3
Answer: D
Question 4
Answer: A
Question 5
Answer: A

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