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Instructor-Guided Lessons and Activities
Learn key objectives through expert-led lectures, discussions, and exercises.
Hands-on practice on Tools
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After Each Session
Q & A Session.
Wrap up the session with clarification on concepts and labs, if needed.
SAS Clinical Data Integration organizes, standardizes and manages clinical research data and metadata. In this module, we will discuss about Research process, different Programming requirement and many more..
Describe the clinical research process (phases, key roles, key organizations)
Interpret a Statistical Analysis Plan.
Accessing, managing and transforming clinical trials data.
Derive programming requirements from an SAP and an annotated Case Report.
Statistical procedures and macro programming.
Reporting clinical trials results.
Describe regulatory requirements (principles of 21 CFR Part 11, International Conference on Harmonization, Good Clinical Practices)
Learn what is the purpose, Structures of CDISC SDTM data model, Different types of clinical trials and also the principles of CDISC.
>> Identify the classes of clinical trials data (demographic, lab, baseline, concomitant medication, etc.)
>> Key personnel in companies must be committed to implementing the CDISC/CDASH standards.
>> Identify key CDISC principles 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
>> Implementing the new standards that involves reorganizing the operations (of an organization) so as to improve efficiency [processes and SOPs].
>> Data management staff [CDM, clinical programmers], biostatisticians, and clinical monitors may find it difficult to converge on a new standard when designing standard libraries and processes.
This session provides an Clincial Trials that can import, export data by using the requirements of SAS V5.
>> Learn how many types of data that are critical for integration.
>> Learn at what point the data should be imported into Express.
>> Apply regulatory requirements to export SAS data sets (SAS V5 requirements).
>> Subsequent data reconciliation process that is required to ensure all integrated data is done so correctly.
>> The impact integration has on exporting data from Express
In this module, we will provide the concept of SQL procedure to access DICTIONARY Tables and also to manage clinical trials as Input data.
>> Role of the clinical data manager in a clinical trial.
>> Access DICTIONARY Tables using the SQL procedure.
>> Examine and explore clinical trials input data (find outliers, missing vs. zero values, etc).
>> Database design and build
* Computer system validation (CSV)
>> Validation rules
>> Serious adverse event reconciliation
>> Metrics and tracking
Here you will learn, how to transform the Clinical Trial Data by applying the ‘observation carry forward’ technique, calculating the results by ‘change from baseline’ and finally how to obtain the count of events in Clinical Trials.
>> Apply categorization and windowing techniques to clinical trials data.
>> Crowd sourcing will transform trial participation
>> 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.
>> Mobile Computing and Data Gathering.
>> Social Media’s Influence on Clinical Trials
Learn, how to apply Statistical Procedures for Clinical Trials, How to use PROC FREQ, PROC TTEST to obtain p-values for categorical and continuous data respectively and also how to create output data sets in SAS Clinical.
>> 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 (2×2 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.
This Macro Clinical sas Programming is especially useful for a large data set and huge time saver. In this session, you have an brief understanding on creation of macro variables, how to call the macros and options used to debug macro and display them in log format.
>> 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).
>> Successful Process Improvement using Validated SAS Macros in Clinical Trial Reporting.
>> Ensuring Usage of Newly Developed Macros.
>> Benefits of New SAS Macros.
This module focuses on how to produce tables and list clinical trial reports using PROC REPORT and ODC global statements respectively.
>> How to Register a Clinical Trial.
>> How to Report Clinical Trial 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.
>> Sharing and Reporting the Results of Clinical Trials - The principle of data sharing dates to the dawn of scientific discovery.
Validation is a critical component to program clinical trial analysis. Essential to effective validation is the programmer’s understanding of the data with which they’ll be working. In this module, you will learn about principles of validation, identify the logic errors and process to resolve them.
>> 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.
>> Reporting and statistics.
Here are Some Statistical Approaches to Analysis of Small Clinical Trials:
>> Sequential analysis
>> Hierarchical models
>> Bayesian analysis
>> Decision analysis
>> Statistical prediction
>> Meta-analysis and other alternatives
>> Risk-based allocation
Have any queries regarding course curriculum, speak to our course advisorConnect with Advisor
Upon successful completion of the program, you will be awarded a Certificate from Mindmajix for Clinical SAS Training.
Successfully complete your course and let the community know about your achievement.
Trainer will cover all the topics related to Certification.
Don’t just show off your achievement to the community, use it to advance in your career.
Have questions? We’ve got the answers. Get the details on how you can grow in this course.
Our trainers have relevant experience in implementing real-time solutions on different queries related to different topics of Clinical SAS. Mindmajix verifies their technical background and expertise.
We record each LIVE class session you undergo through and we will share the clinical sas training videos / recording of each session/class.
Trainer will provide the Environment/Server Access to the students and we ensure practical real-time experience and training by providing all the utilities required for the in-depth understanding of the course.
If you are enrolled in classes and/or have paid fees, but want to cancel the registration for certain reason, it can be attained within 48 hours of initial registration. Please make a note that refunds will be processed within 30 days of prior request.
There are some Group discounts available if the participants are more than 2.
As we are one of the leading providers of Live Instructor LED SAS Clinical Training, We have customers from USA, UK, Canada, Australia, UAE, Qatar, NZ, Singapore, Malaysia, India and other parts of the world. We are located in USA. Offering Online SAS Clinical Training in Cities like:
New York, New jersey, Dallas, Seattle, Baltimore, Houston, Minneapolis, Los Angeles, San Francisco, San Jose, San Diego, Washington DC, Chicago, Philadelphia, St. Louis, Edison, Jacksonville, Towson, Salt Lake City, Davidson, Murfreesboro, Atlanta, Alexandria, Sunnyvale, Santa clara, Carlsbad, San Marcos, Franklin, Tacoma, California, Bellevue, Austin, Charlotte, Garland, Raleigh-Cary, Boston, Orlando, Fort Lauderdale, Miami, Gilbert, Tempe, Chandler, Scottsdale, Peoria, Honolulu, Columbus, Raleigh, Nashville, Plano, Toronto, Montreal, Calgary, Edmonton, Saint John, Vancouver, Richmond, Mississauga, Saskatoon, Kingston, Kelowna, Hyderabad, Bangalore, Pune, Mumbai, Delhi, Dubbai, Doha, Melbourne, Brisbane, Perth, Wellington, Auckland etc…
SAS Clinical specializes in organizing, standardizing and managing critical research data and metadata. With SAS course, both speed and efficiency is gained by automating constant clinical trial data integration tasks.
Here are the list of SAS Clinical Course Objectives:
Proficient Programming skills in Clinical SAS
Register source data and target tables
Enhance table relationships using integrity constraints, key, and indexes
Create custom transformation
Clinical study Documents
Clinical SAS Data Integration
Compliance, Auditing & Quality Control in Clinical Research
Related Jobs and Positions in the Industry
The clinical sas online course provides a solid foundation in defining analysis data sets and strategic analyses viz. cross-study and advanced safety analysis. Using the clinical features, target table metadata of clinical domain is built to support the structure and content of the clinical domains based on the standards.
As such there are no prerequisites for learning SAS Clinical. However, with a number of opportunities in the field, the following job roles will get benefited from this course:
Clinical SAS Business Analyst
SAS Clinical Data Programmer/Manager
SAS Data Management Professionals
Data Warehousing Professionals
SAS Clinical Project Manager
Clinical Sas Programmer
SAS Clinical Quality Analyst
SAS ETL Specialist
Business Intelligence Professionals
An in-depth knowledge of an SAS Clinical project ensures all the critical components of Clinical are covered by our trainer. With this information, you can increase your visibility and enhance your efficiency in drawing real connections among different components of SAS Clinical. We will also enable the complete material covering all the aspects of this project.
>> Clinical SAS Programmer - $74,789
>> Senior SAS Clinical Trials Programmer - $88,126
>> SAS Clinical Analyst - $70,992
Disclaimer- The information in above graph on salary trends mentioned above has been collected to various sources. It may not be same across the globe.
How to get certified in SAS Clinical?
SAS Clinical Trail Certification credentials are popular worldwide as behaves as a primary means to authenticate SAS knowledge. Clinical SAS Certification sets the individuals apart from others and acts as a proof of SAS knowledge. It definitely makes a difference within an organization. Some of the major certification exams include:
>> SAS Certified Clinical Trials Programmer Using SAS 9
>> Clinical Trials Programming Using SAS 9 – Accelerated Version.
These certifications can help candidates aspire for their rewarding clinical sas programmer jobs for freshers as well experienced. By opting for our well-structured training at Mindmajix, candidates can gain knowledge to enter the lucrative domain of SAS Clinical and earn the certification.
For more information regarding various types of clincal sas certification available, please go through the SAS Clinical Certification.
MindMajix SAS Clinical Course Completion Certificate
Mindmajix guarantees that the educational experience you gain will deliver value even after you complete the course with its course completion certificate. This will undoubtedly be one of the valuable certifications for your career path and your first step in building a career in this course. You can earn this after successful completion of your project work and can get your CV noticed. It also shows you are motivated to learn and that you have genuine expertise.
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