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SASInstitute A00-281 Actual Tests : SAS Certified Clinical Trials Programmer Using SAS 9 Accelerated Version
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For Clinical Trials Programming Using SAS 9 Accelerated Version (A00-281) Certification Exam here is the study guide
Clinical Trials Programming Using SAS 9 Accelerated Version (A00-281): Get our quick guide if you don't have time to read all the page
The SAS Certified Clinical Foundation Accelerated Version certification is considered the reference point for knowledge, skills and proven ability to identify classes of clinical study data (demographic, laboratory and reference data. The SAS Clinical Foundation Accelerated Version certification is a certification a very important passage in the A00-281 program of the SAS Institute certification hierarchy for the planning of clinical studies using the credentials of the accelerated version of SAS 9 confirms that you have a solid knowledge base on the fundamentals of computer science and to support the accelerated version SAS Certified Clinical Foundation For this, it is necessary to eliminate SAS Institute A00-281 Planning of clinical studies using the accelerated version of SAS 9. Exam A00-281 (Planning of clinical studies with version a This SAS 9 Accelerated is one of the fundamental computer exams that must be passed for obtaining certification for the accelerated version of the SAS Certified Clinical Foundation.
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Salary of Clinical Trials Programming Using SAS 9 Accelerated Version (A00-281) Certified Professional
The price of Clinical Trials Programming Using SAS 9 Accelerated Version (A00-281) exam is $180 USD.
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SASInstitute A00-281 Exam Syllabus Topics:
| Section | Weight | Objectives |
|---|---|---|
| Topic 1: Clinical Trials Programming Concepts | - CDISC standards and clinical data structures - Clinical trial programming standards and practices | |
| Topic 2: Transform or Summarize Clinical Trials Data | 15% | - Use SAS DATA step programming techniques - Create derived datasets and variables |
| Topic 3: Macro Programming for Clinical Trials | 15% | - Automate clinical programming tasks - Create and use SAS macros |
| Topic 4: Regulatory Submissions | 5% | - Prepare data and documentation for regulatory submission |
| Topic 5: Apply Statistical Procedures for Clinical Trials | 15% | - Analyze clinical trial data - Use SAS statistical procedures |
| Topic 6: Report Clinical Trials Results | 10% | - Create clinical trial reports - Produce tables, listings, and reports |
| Topic 7: Validate Clinical Trial Data Reporting | 20% | - Perform quality control programming - Validate clinical trial outputs |
| Topic 8: Manage Clinical Trials Data | 5% | - Import, access, and manage clinical trial data - Apply clinical data management concepts |
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