SAS A00-281 Certification Exam Syllabus

A00-281 Syllabus, A00-281 PDF Download, SAS A00-281 Dumps, SAS Clinical Trials Programmer - Accelerated Version PDF Download, SAS Certified Clinical Trials Programmer Using SAS 9 - Accelerated Version Certification

This page is a one-stop solution for any information you may require for SAS Certified Clinical Trials Programmer Using SAS 9 - Accelerated Version (A00-281) Certification exam. The SAS A00-281 Exam Summary, Syllabus Topics and Sample Questions provide the base for the actual SAS Certified Clinical Trials Programmer - Accelerated Version exam preparation, we have designed these resources to help you get ready to take your dream exam.

The SAS Certified Clinical Trials Programmer Using SAS 9 - Accelerated Version credential is globally recognized for validating SAS Clinical Trials Programmer - Accelerated Version knowledge. With the SAS Certified Clinical Trials Programmer - Accelerated Version Certification credential, you stand out in a crowd and prove that you have the SAS Clinical Trials Programmer - Accelerated Version knowledge to make a difference within your organization. The SAS Certified Clinical Trials Programmer Using SAS 9 - Accelerated Version Certification (A00-281) exam will test the candidate's knowledge on following areas.

SAS A00-281 Exam Summary:

Exam Name SAS Certified Clinical Trials Programming - Accelerated Version
Exam Code A00-281
Exam Duration 120 minutes
Exam Questions 70 to 75 multiple-choice and short-answer questions
Passing Score 70%
Exam Price $180 (USD)
Training
Books Clinical Trials: A Practical Guide to Design, Analysis, and Reporting
Exam Registration Pearson VUE
Sample Questions SAS Clinical Trials Programming - Accelerated Version Certification Sample Question
Practice Exam SAS Clinical Trials Programming - Accelerated Version Certification Practice Exam

SAS A00-281 Exam Topics:

Objective Details
Clinical Trials Process
- Describe the clinical research process (phases, key roles, key organizations)
- Interpret a Statistical Analysis Plan
- Derive programming requirements from an SAP and an annotated Case Report Form
- Describe regulatory requirements (principles of 21 CFR Part 11, International Conference on Harmonization, Good Clinical Practices)
Clinical Trials Data Structures
- Identify the classes of clinical trials data (demographic, lab, baseline, concomitant medication, etc)
- Identify key CDISC principals and terms
- Describe the structure and purpose of the CDISC SDTM data model
- Describe the structure and purpose of the CDISC ADaM data model
- Describe the contents and purpose of definexml
Import and Export Clinical Trials Data
- Apply regulatory requirements to exported SAS data sets (SAS V5 requirements)
Manage Clinical Trials Data
- Access DICTIONARY Tables using the SQL procedure
- Examine and explore clinical trials input data (find outliers, missing vs zero values, etc)
Transform Clinical Trials Data
- Apply categorization and windowing techniques to clinical trials data
- Transpose SAS data sets
- Apply 'observation carry forward' techniques to clinical trials data (LOCF, BOCF, WOCF)
- Calculate 'change from baseline' results
- Obtain counts of events in clinical trials
Apply Statistical Procedures for Clinical Trials
- Use SAS procedures to obtain descriptive statistics for clinical trials data (FREQ, UNIVARIATE, MEANS, SUMMARY)
- Use PROC FREQ to obtain p-values for categorical data (2x2 and NxP test for association)
- Use PROC TTEST to obtain p-values for continuous data (one-sample, paired and two-sample t-tests)
- Create output data sets from statistical procedures
Macro Programming for Clinical Trials
- Create and use user-defined and automatic macro variables
- Automate programs by defining and calling macros
- Use system options to debug macros and display values of macro variables in the SAS log (MPRINT, SYMBOLGEN, MLOGIC, MACROGEN)
Report Clinical Trials Results
- Use PROC REPORT to produce tables and listings for clinical trials reports
- Use ODS and global statements to produce and augment clinical trials reports
Validate Clinical Trial Data Reporting
- Explain the principles of programming validation in the clinical trial industry
- Utilize the log file to validate clinical trial data reporting
- Use programming techniques to validate clinical trial data reporting (PROC COMPARE, MSGLEVEL)
- Identify and Resolve data, syntax and logic errors

The SAS has created this credential to assess the knowledge and understanding of a candidate in the area as above via the certification exam. The SAS Clinical Trials Programmer - Accelerated Version (A00-281) Certification exam contains a high value in the market being the brand value of the SAS attached with it. It is highly recommended to a candidate to do a thorough study and also get a hand full of the practice to clear SAS Certified Clinical Trials Programmer Using SAS 9 - Accelerated Version exam without any hiccups.

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