SAS Certified Clinical Trials Programmer Using SAS 9 (A00-281)

The SAS Certified Clinical Trials Programmer Using SAS 9 A00-281 credential is globally acknowledged for validating SAS Clinical Trials Programming knowledge. With the SAS Certified Clinical Trials Programming credential, the candidate stands out in a crowd and prove that they have the SAS Clinical Trials Programming Using SAS 9 A00-281 knowledge to make a difference within your organization. The SAS Certified Clinical Trials Programmer Using SAS 9 validates a candidates’ ability to apply SAS® programming skills to clinical trial data. The exam tests the understanding and knowledge related to topics such as clinical trial process, accessing, managing, and transforming clinical trial data, statistical procedures, and macro programming, reporting clinical trial results, validating clinical trial data reporting.

Successful candidates should be skilled in tasks such as:

Clinical trial process.
Accessing, managing, and transforming clinical trials data.
Statistical procedures and macro programming.
Reporting clinical trials results.
Validating clinical trial data reporting.

Benefits of SAS Credentials:

Validate your skills. Stand out.

Earn recognition for your knowledge.
Increase your value to your employer.
Enhance your credibility as a SAS professional.
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Learning Path

SAS offers a variety of certifications in areas such as Foundation tools, Advanced analytics, BI and Analytics, Data Management, Administration, JMP, and more. SAS Certified Architecture and Design Specialist exams are part of the Partners category.

Learning Objectives

The objectives for the SAS Certified Clinical Trials Programmer Using SAS 9 A00-281 are:

Clinical Trials Process
Clinical Trials Data Structures
Import and Export Clinical Trials Data
Manage Clinical Trials Data
Transform Clinical Trials Data
Apply Statistical Procedures for Clinical Trials
Macro Programming for Clinical Trials
Report on Clinical Trials Results
Validate Clinical Trial Data Reporting

Exam Details

SAS and Pearson VUE jointly deliver the SAS Certified Clinical Trials Programmer Using SAS 9 test, which has the ID (A00-281).
The exam consists of 70-75 multiple-choice questions, and passing the exam requires a score of at least 70%.
The SAS Certified Clinical Trials Programmer Using SAS 9 A00-281 exam will take 2 hours, or 120 minutes to complete.

Scheduling the Exam:

The candidate needs to register for the exam at Pearson VUE. The exam ID i.e A00-281 will be required while registering. The exam fee is $180 USD in India and most other countries.

SAS Certified Clinical Trials Programmer Using SAS 9 (A00-281) FAQ

For more details visit SAS Certified Clinical Trials Programmer Using SAS 9 A00-281 FAQ

Course Outline

SAS has divided the syllabus into various sections. The SAS Certified Clinical Trials Programmer Using SAS 9 A00-281 exam includes its objectives and sub-topics in it. The detailed course outline is mentioned below:

1. 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).

2. Clinical Trials Data Structures

Identify the classes of clinical trial data (demographic, lab, baseline, concomitant medication, etc.).
Identify key CDISC principals and terms.
Describe the structure and purpose of the CDISC SDTM data model.
Describing the structure and purpose of the CDISC ADaM data model. (SAS Documentation: Preparing Analysis Data Model (ADaM))
Describe the contents and purpose of define.xml. (SAS Documentation: Understanding the define.xml File)

3. Import and Export Clinical Trials Data

Apply regulatory requirements to exported SAS data sets (SAS V5 requirements).

4. Manage Clinical Trials Data

Access DICTIONARY Tables using the SQL procedure. (SAS Documentation: Accessing SAS Information By Using DICTIONARY Tables)
Examine and explore clinical trials input data (find outliers, missing vs. zero values, etc). (SAS Documentation: Outlier Detection, MISSING Statement)

5. Transform Clinical Trials Data

Apply categorization and windowing techniques to clinical trials data. (SAS Documentation: Running Programs in the SAS Windowing Environment)
Transpose SAS data sets. (SAS Documentation: TRANSPOSE Procedure)
Apply ‘observation carry forward’ techniques to clinical trials data (LOCF, BOCF, WOCF).
Calculate ‘change from baseline’ results.
Obtain counts of events in clinical trials.

6. Apply Statistical Procedures for Clinical Trials

Use SAS procedures to obtain descriptive statistics for clinical trials data (FREQ, UNIVARIATE, MEANS, SUMMARY). (SAS Documentation: FREQ Procedure, MEANS Procedure, UNIVARIATE Procedure, SUMMARY Procedure)
Use PROC FREQ to obtain p-values for categorical data (2×2 and NxP test for association). (SAS Documentation: The FREQ Procedure)
Use PROC TTEST to obtain p-values for continuous data (one-sample, paired, and two-sample t-tests). (SAS Documentation: TTEST Procedure)
Create output data sets from statistical procedures. (SAS Documentation: FREQ Procedure)

7. Macro Programming for Clinical Trials

Create and use user-defined and automatic macro variables. (SAS Documentation: Macro Variables Defined by Users)
Automate programs by defining and calling macros. (SAS Documentation: Defining and Calling Macros)
Use system options to debug macros and display values of macro variables in the SAS log (MPRINT, SYMBOLGEN, MLOGIC, MACROGEN). (SAS Documentation: Debugging Techniques)

8. Report of Clinical Trials Results

Use PROC REPORT to produce tables and listings for clinical trials reports. (SAS Documentation: REPORT Procedure)
Use ODS and global statements to produce and augment clinical trials reports. (SAS Documentation: Global Statements, ODS DOCUMENT Statement)

9. Validate Clinical Trial Data Reporting

SAS Documentation: 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.

Exam Policies

The candidate should visit the SAS official website for understanding the terms and policies. The exam terms and policies include various important information such as age requirements and policies concerning minors, candidate identification, and authentication, rights and responsibilities, Confidentiality and agreements, etc.

Preparatory Guide for SAS Certified Clinical Trials Programmer Using SAS 9 (A00-281) Exam

The preparation steps which are essential in order to successfully pass the SAS Certified Clinical Trials Programmer Using SAS 9 A00-281 exam. To improve your chances, we equip you with a study guide with expert learning resources and a practise exam. Official learning tools and practise tests are included to help you prepare. Let’s get the study guide underway.

SAS Certified Clinical Trials Programmer Using SAS 9 A00-281 preparatory guide

1. SAS Official Website

While studying for the SAS Certified Clinical Trials Programmer Using SAS 9 A00-281 exam, it is critical to visit the SAS official website. The official site has a wealth of reliable information and resources that may be used to prepare for the exam. The resources such as study guide, documentation, sample papers, flashcards, whitepapers, sample questions, faqs, etc. The candidate can find all such important things on the official page.

2. SAS Training Program

Training programs are a very necessary step in the preparation for such exams as the SAS Certified Clinical Trials Programmer Using SAS 9 A00-281. Further, this offers its own training programs on its various examinations and certifications.

3. Flashcards

With quiz-style printable flashcards, candidates may test their knowledge of the SAS Certified Clinical Trials Programmer Using SAS 9 A00-281 exam. Furthermore, the SAS Certified Clinical Trials Programmer Using SAS 9 study flashcards highlights the most important learning topics from the study guide. CLICK HERE for flashcards!

4. Books and Guides

Books and study guides should be the following stage in the preparation process. The aspirant must seek for books that are full of useful knowledge. Finding a decent book may be tough, but the candidate must discover, read, and comprehend in order to gain information and abilities. The following are some options for the candidate to consider:

Learning SAS by Example: A Programmer’s Guide, Second Edition by Ron Cody

The candidate can find more SAS books here!

5. Join a Study Group

Participating in a group study will also benefit the candidate. It will motivate them to put in more effort. Additionally, studying in a group will allow them to maintain contact with others who are on the same route as them. Furthermore, the conversation in such study groups will assist students in passing their tests.

6. Practice Test

Most importantly, candidates have to try their hands-on practice tests. Practice tests are the one who secures the candidate about their preparation. The practice test will help the candidates to recognize their vulnerable areas so that they can work on them. There are many practice tests available on the internet nowadays, so the candidate can choose which they want.