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SASInstitute Clinical Trials Programming Using SAS 9.4 Sample Questions:

1. 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 the pharmacovigilance, pharmacokinetics, and pharmacodynamics of a drug
D) designed to assess how well the drug works and further assess safety

2. This question will ask you to provide a missing option.
The following program is submitted to create a transport file for multiple data sets:

Which option will limit the files that are copied to type data?

A) entrytype=data
B) intype=data
C) memtype=data
D) include=data

3. Which code segment includes a statement that would reset the graphics counter and ensure a 6in by
4in image is produced?

A) ods graphics / counter = 1 width = 6in height = 4in;
B) ods graphics / width = 6in height = 4in counter = 1;
C) ods graphics / width = 6in height = 4in reset;
D) ods graphics / reset width = 6in height = 4in;

4. What is the primary purpose for specifying identifier variables across SDTM domains?

A) To include the appropriate subject information
B) To satisfy regulatory conditions
C) To include the appropriate study information
D) To uniquely reference each record

5. You are working on validating the ADSL data set which contains the variables subject, sex, age, birth date, baseline height, and baseline weight. These variables are brought in from SDTM, and you derive new variables baseline BMI (from baseline height and weight) and age categorization (from age).

You get the following in the SAS log:

To reconcile this difference, which variable values will be most helpful to provide to the production programmer?

A) BLBMI
B) AGECAT1 BLBMI
C) SUBJID BLHT BLWT BLBMI
D) SUBJID BLBMI

Solutions: