SASInstitute A00-282: Clinical Trials Programming Using SAS 9.4 is an important certification for individuals who work in the field of clinical trials programming. A00-282 exam tests the knowledge and skills of candidates in various areas of clinical trials programming, including data management, statistical analysis, and report generation. Clinical Trials Programming Using SAS 9.4 certification is recognized by many pharmaceutical companies as a standard for hiring SAS programmers for clinical trials programming positions, and it is beneficial for individuals who want to enhance their skills and knowledge in this field.
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SASInstitute A00-282 exam is recommended for clinical programmers, biostatisticians, data managers, and others who work within the pharmaceutical and biotech industries. A00-282 exam consists of 85 multiple-choice questions and must be completed within 2 hours and 15 minutes. A00-282 exam is available in English and costs $180 USD to take. Upon passing the exam, individuals will receive a SASInstitute Certificate in Clinical Trials Programming Using SAS 9.4, which can help to distinguish them from other professionals in the field.
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SASInstitute A00-282 exam is designed to test the knowledge and skills of individuals in the field of clinical trials programming using SAS 9.4. SAS is a powerful statistical software package used in the healthcare industry to manage and analyze large amounts of clinical trial data. A00-282 exam covers a wide range of topics, including data management, analysis and reporting, as well as SAS programming techniques.
SASInstitute A00-282 (Clinical Trials Programming Using SAS 9.4) Certification Exam is a globally recognized certification that validates an individual's expertise in SAS programming for clinical trials. Clinical Trials Programming Using SAS 9.4 certification is intended for individuals who work in the pharmaceutical industry, contract research organizations (CROs), or academic research organizations (AROs) and are involved in the programming and analysis of clinical trial data.
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| Section | Weight | Objectives |
|---|---|---|
| Topic 1: Manage Clinical Trials Data | 5% | - Clean, merge, and subset data - Use SQL and dictionary tables - Access and explore clinical datasets |
| Topic 2: Report Clinical Trials Results | 10% | - Produce tables, listings, and figures - PROC REPORT and PROC PRINT |
| Topic 3: Transform or Summarize Clinical Trials Data | 15% | - Aggregation and transposition - Derive variables and study days - Data step manipulation |
| Topic 4: Macro Programming for Clinical Trials | 15% | - Create and call macros - Debugging macros - Macro variables and parameters |
| Topic 5: Validate Clinical Trial Data Reporting | 20% | - Use PROC COMPARE and log review - Programming validation techniques - Validation principles |
| Topic 6: Regulatory Submissions | 5% | - ICH and FDA guidelines - Compliance for clinical data reporting |
| Topic 7: Clinical Trials Process | 5% | - Derive programming requirements from protocol and CRF - Clinical trial lifecycle and protocol |
| Topic 8: Apply Statistical Procedures for Clinical Trials | 15% | - Basic statistical analysis for clinical data - PROC MEANS, FREQ, TABULATE |
| Topic 9: Clinical Trials Data Structures | 10% | - Clinical domain structures - Define.xml and dataset specifications - CDISC standards: SDTM, ADaM |
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