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SASInstitute A00-282 Exam Syllabus Topics:

Section

Objectives

Topic 1: Clinical Trials Data Standards

- CDISC Standards

1. ADaM datasets and analysis-ready data
2. SDTM structure and implementation

Topic 2: Regulatory and Clinical Research Concepts

- Clinical trial workflow

1. Regulatory submission basics
2. Study design fundamentals

Topic 3: SAS Programming for Clinical Trials

- Data Management

1. Dataset merging and manipulation
2. Data cleaning and transformation

- Reporting and Analysis

1. Statistical reporting with SAS procedures
2. Listings, tables, and figures generation

SASInstitute Clinical Trials Programming Using SAS 9.4 Sample Questions:

1. In PROC REPORT, which usage creates a column in the report for each distinct formatted value of the variable listed in the DEFINE statement?

A) ACROSS
B) ANALYSIS
C) DISPLAY
D) GROUP

2. 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

3. What is the main focus of 21 CFR Part 11?

A) statistical calculation requirements
B) electronic submission requirements
C) trial protocol requirements
D) trial safety requirements

4. The following SAS program is submitted:

You want to store all calculated means and standard deviations in one SAS data set.
Which statement must be added to the program?

A) output out=WORK.RESULTS mean=m1 m2 std=s1 s2;
B) ods output mean=m1 m2 std=s1 s2;
C) output mean std;
D) ods output out=WORK.RESULTS mean=m1 m2 std=s1 s2;

5. Which percentage in the table is calculated incorrectly, assuming the cell counts are correct?
Percentages are rounded to the nearest whole percent.