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SASInstitute Clinical Trials Programming Using SAS 9.4 Sample Questions:

1. Given the following two data sets EX and AE:

Which output data set is produced by the submitted SAS program?

A) Option C
B) Option D
C) Option A
D) Option B

2. When writing a validation program using independent programming, which two actions conform to good programming practices?
(Choose two.)

A) Delete subjects from the production side that are causing differences with the validation data set.
B) Copy statistical code directly from the production program.
C) Copy statistical code directly from the SAP.
D) Ensure the production program has been run prior to compare.

3. Which statement correctly describes an aspect of a Phase II clinical trial?

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

4. Review the following procedure code:
proc ttest data=DATA1;
class GROUPVAR1;
var VAR1;
run;
Which variable is most appropriate to be analyzed as variable VAR1?

A) Age, with possible values of any integer between and including 18 and 65
B) Treatment, with possible values of "Placebo" or "Active"
C) Number of infections, with possible values of 0, 1, or 2
D) Systolic blood pressure, with possible values of "<120", "120 - 139", "140 - 159", "160 - 179", and
"180+"

5. What is the definition for treatment-emergent adverse event (TEAE)?

A) AE that continued after the first dose of study drug
B) AE that started or worsened after the first dose of study drug
C) AE that improved after the first dose of study drug
D) AE that started 6 months after the last dose of study drug

Solutions: