This page is a one-stop solution for any information you may require for SAS Certified Clinical Trials Programming 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 Programming - Accelerated Version exam preparation, we have designed these resources to help you get ready to take your dream exam.
The SAS Certified Clinical Trials Programming Using SAS 9 - Accelerated Version credential is globally recognized for validating SAS Clinical Trials Programming - Accelerated Version knowledge. With the SAS Certified Clinical Trials Programming - Accelerated Version Certification credential, you stand out in a crowd and prove that you have the SAS Clinical Trials Programming - Accelerated Version knowledge to make a difference within your organization. The SAS Certified Clinical Trials Programming 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 Using SAS 9 - Accelerated Version |
| Exam Code | A00-281 |
| Exam Duration | 120 minutes |
| Exam Questions | 70-75 |
| Passing Score | 70% |
| Exam Price | $180 (USD) |
| Training |
SAS Macro Language 1: Essentials SAS Report Writing 1: Essentials Statistics 1: Introduction to ANOVA, Regression, and Logistic Regression |
| Books |
SAS Programming in the Pharmaceutical Industry Clinical Trials: A Practical Guide to Design, Analysis, and Reporting Introducing the CDISC Standards: New Efficiencies for Medical Research Validating Clinical Trial Data Reporting with SAS Implementing CDISC Using SAS: An End-to-End Guide |
| 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 define.xml. |
| 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 Programming - 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 Programming Using SAS 9 - Accelerated Version exam without any hiccups.