Udemy – Clinical SAS Programming(CDISC)
Udemy – Clinical SAS Programming(CDISC)
MP4 | Video: 1280x720 | 67 kbps | 44 KHz | Duration: 7 Hours | 713 MB
Genre: eLearning | Language: English
MP4 | Video: 1280x720 | 67 kbps | 44 KHz | Duration: 7 Hours | 713 MB
Genre: eLearning | Language: English
Learn CDISC Standards for SAS Programming with basic overview of clinical trials and applying SAS programming skills
This course is designed to teach important concepts related to clinical sas programming which is a blend of base sas, advance sas & CDISC SDTM standards. The course focuses on
Week 1: A basic overview of clinical research
·Describe the clinical research process (phases, key roles, and key organizations).
·Describe regulatory requirements (principles of 21 CFR Part 11, International Conference on Harmonization, Good Clinical Practices).
Week 2: An introduction to CDISC standards and implementation of SDTM principles
·Overview of CDISC and its standards like CDASH,ODM, SDTM, ADAM
·Describe the structure and purpose of the CDISC SDTM data model
·Annotate CRF as per CDISC standards
·Convert Non-CDISC dataset to CDISC compliance datasets
·Describe the contents and purpose of define file
Week 3-Managing and Transforming techniques -Base SAS
·Introduction-Basic overview of SAS software
·Reading SAS datasets-Descriptor & Data portions
·Creating SAS Datasets
·Manipulating data- Variable creation, Subsetting Observation
·Combining SAS Datasets
·Appending, concatenating dataset
·Merging the SAS dataset
·Append data in existing data files
Week 4: Applying statistical procedures
·Use SAS procedures to obtain descriptive statistics for clinical trials data (FREQ, UNIVARIATE, MEANS, and SUMMARY).
Week 5: SAS Macro Language-Advance SAS
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, and MACROGEN).
What are the requirements?
• No experience with SAS is required • Basic computer skills are required. • Familiarity with clinical terminology is advantageous, although not essential
What am I going to get from this course?
Over 45 lectures and 6.5 hours of content!
Course Goal: This course will enable you to be a competent Clinical SAS Programmer with knowledge of CDISC
Course Objectives: In this course, you will be able to learn • Clinical research process and associated regulatory guidelines • CDISC standards and applying SDTM principles to clinical research data • Managing, and transforming clinical trials data with sas techniques • Implementing descriptive statistical procedures and macro programming
What is the target audience?
• Course intended for every aspirant who wants to make a career in Clinical SAS Programming • Refresher course, for programmers working in Pharmaceutical industry or CRO’s
·Annotate CRF as per CDISC standards
·Convert Non-CDISC dataset to CDISC compliance datasets
·Describe the contents and purpose of define file
Week 3-Managing and Transforming techniques -Base SAS
·Introduction-Basic overview of SAS software
·Reading SAS datasets-Descriptor & Data portions
·Creating SAS Datasets
·Manipulating data- Variable creation, Subsetting Observation
·Combining SAS Datasets
·Appending, concatenating dataset
·Merging the SAS dataset
·Append data in existing data files
Week 4: Applying statistical procedures
·Use SAS procedures to obtain descriptive statistics for clinical trials data (FREQ, UNIVARIATE, MEANS, and SUMMARY).
Week 5: SAS Macro Language-Advance SAS
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, and MACROGEN).
What are the requirements?
• No experience with SAS is required • Basic computer skills are required. • Familiarity with clinical terminology is advantageous, although not essential
What am I going to get from this course?
Over 45 lectures and 6.5 hours of content!
Course Goal: This course will enable you to be a competent Clinical SAS Programmer with knowledge of CDISC
Course Objectives: In this course, you will be able to learn • Clinical research process and associated regulatory guidelines • CDISC standards and applying SDTM principles to clinical research data • Managing, and transforming clinical trials data with sas techniques • Implementing descriptive statistical procedures and macro programming
What is the target audience?
• Course intended for every aspirant who wants to make a career in Clinical SAS Programming • Refresher course, for programmers working in Pharmaceutical industry or CRO’s
Udemy – Clinical SAS Programming(CDISC)
