How can you study for the Clinical Trials Programming Using SAS 9 Accelerated Version (A00-281) Certification Exam

For Clinical Trials Programming Using SAS 9 Accelerated Version (A00-281) Certification Exam here is the study guide

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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.

Here are the topics of Clinical Trials Programming Using SAS 9 Accelerated Version (A00-281) Exam

Candidates must know the exam topics before they start of preparation. Because it will really help them in hitting the core. Our Clinical Trials Programming Using SAS 9 Accelerated Version A00-281 exam dumps will include the following topics:

Clinical Trials Process

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

Here is a procedure to register for the Clinical Trials Programming Using SAS 9 Accelerated Version (A00-281) Exam

In order to apply for the Clinical Trials Programming Using SAS 9 Accelerated Version (A00-281), You have to follow these steps

• Step 1: Visit to Pearson Exam Registration
• Step 2: Signup/Login to Pearson VUE account
• Step 3: Search for SAS Business Analytics Administration (A00-250) Exam Certifications Exam
• Step 4: Select Date, time and confirm with payment method

Reference: https://www.sas.com/en_us/certification/credentials/foundation-tools/clinical-trials-programmer/clinical-trials-programming-accelerated-exam.html

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