Clinical SAS Programmer Training in Pro Career
Develop your Skills throughout your convenient time & get practical online training by our Experienced Instructors.More than 90% students has satisfied from our instructors & hands on Experience in SAS Clinical Base Programming,SAS Clinical Analysis.
Collaborative Learning and Career Building
At the end of most Clinical SAS Programmer Training lessons, you'll have access to an online discussion. Engaging actively and constructively in these discussions can significantly boost your SAS Clinicals career development. By offering help or seeking assistance from the trainers, you’ll build meaningful relationships and create valuable professional connections.
These discussions are more than just a conversation to share ideas—they're designed to accelerate your SAS Clinicals learning journey. That's why it is made an essential part of our courses: to support your growth and help you enhance your SAS Clinicals skills through collaboration and shared insights.
Advantages of enrolling up for Clinical SAS Programmer Training

- Online Training
- Classroom Training
- Placements
Details to know about Clinical SAS Programmer Training

SAS Clinicals Training with Placement
Course Content:
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:
- Combine SAS data sets.
- Efficiently import and subset SAS data sets.
- Access data in an Excel workbook (LIBNAME and PROC IMPORT/EXPORT).
- Create temporary and permanent SAS data sets.
- Apply regulatory requirements to exported SAS data sets (SAS V5 requirements).
Manage Clinical Trials Data:
- Investigate SAS data libraries using base SAS utility procedures (PRINT, CONTENTS, FREQ).
- Access DICTIONARY Tables using the SQL procedure.
- Sort observations in a SAS data set.
- Create and modify variable attributes using options and statements in the DATA step.
- Examine and explore clinical trials input data (find outliers, missing vs. zero values, etc).
Transform Clinical Trials Data:
- Process data using DO LOOPS.
- Process data using SAS arrays.
- Retain variables across observations.
- Use assignment statements in the DATA step.
- Apply categorization and windowing techniques to clinical trials data.
- Use SAS functions to convert character data to numeric and vice versa.
- Use SAS functions to manipulate character data, numeric data, and SAS date values.
- 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.
FAQs Clinical SAS Programmer Training from Pro Career
Where is the course conducted?
The Clinical SAS Programmer Training is conducted from Brunswick to attend in online, accessible via a dedicated platform from anywhere.
What are the available learning modes for Clinical SAS Programmer Training?
Pro Career offers online and hybrid learning options
What facilities are provided for students enrolled in this course?
Pro Career offers access to online resources, expert lectures, practical labs, student support community, 100% Job assistance and Guaranteed classes.
Who will be conducting the training for this course?
The training for Clinical SAS Programmer Training will be conducted by experienced industry professionals, subject matter experts and certified instructors.
What topics are covered in the course curriculum?
The course covers topics according to the skills and understanding you have on the subject.
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