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SAS A00-280 Exam Questions
- Topic 1: Apply regulatory requirements to exported SAS data sets/ Efficiently import and subset SAS data sets
- Topic 2: Explain the principles of programming validation in the clinical trial industry/ Identify key CDISC principals and terms
- Topic 3: Use programming techniques to validate clinical trial data reporting/ Derive programming requirements from an SAP and an annotated Case Report Form
- Topic 4: Use ODS and global statements to produce and augment clinical trials reports/ Investigate SAS data libraries using base SAS utility procedures
- Topic 5: Examine and explore clinical trials input data/ Describe the clinical research process
- Topic 6: Identify the classes of clinical trials data/ Describe the structure and purpose of the CDISC SDTM data model
- Topic 7: Use PROC REPORT to produce tables and listings for clinical trials reports/ Describe the structure and purpose of the CDISC ADaM data model
- Topic 8: Create and use user-defined and automatic macro variables/ Interpret a Statistical Analysis Plan
- Topic 9: Create and modify variable attributes using options and statements in the DATA step/ Use SAS functions to convert character data to numeric and vice versa
- Topic 10: Apply categorization and windowing techniques to clinical trials data/ Apply 'observation carry forward' techniques to clinical trials data
- Topic 11: Use PROC TTEST to obtain p-values for continuous data/ Create output data sets from statistical procedures/ Clinical Trials Data Structures
- Topic 12: Use SAS procedures to obtain descriptive statistics for clinical trials data/ Access DICTIONARY Tables using the SQL procedure
Free SAS A00-280 Exam Actual Questions
Note: Premium Questions for A00-280 were last updated On 30-08-2024 (see below)
This question will ask you to provide lines of missing code.
Which ODS statements, inserted respectively in the two locations indicated above, create a report stored in a PDF file?
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:
Given the following SAS program:
Which statement correctly identifies invalid values in the variable TRT, if only the values 'A', B', 'C are valid?
A Statistical Analysis Plan describes a clinical trial as "A 12 week, double-blind, placebo-controlled, randomized, multi-center study." Double-blind refers to which groups in this study?
Given the following SAS program:
Which statement correctly identifies invalid values in the variable TRT, if only the values 'A', B', 'C are valid?
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