SAS® Clinical Data Analysis and Reporting for Clinical Trials
This course trains you to analyze, interpret, and report clinical trial data using SAS. Learn advanced statistical methods, generate regulatory-compliant reports, and gain practical skills for roles in clinical research, pharmaceuticals, and healthcare analytics.
About The Program
Gain hands-on expertise in managing and analyzing clinical trial data with SAS. Master SDTM, ADaM, and TLF standards to meet global regulatory requirements and build a strong career in pharmaceutical and healthcare analytics.
COURSE DURATION : 45 hours | Prepares you for the SAS Clinical Trials Programmer Certification exam
Your Learning Journey
- SAS Report Writing: Essentials
- Data Visualization Using SAS ODS Graphics
- Statistics: Introduction to Anova, Regression and Logistic Regression
- Analysis of Clinical Trials
- Generate TLFs for regulatory submissions
- Introduce Define-xml for submission readiness
- Validating Outputs
- Clinical Trial Data Analysis using Statistical Procedures
Additionally, the curriculum builds cross-functional capabilities for clinical research roles through self-paced learning in: Data Literacy | SAS Analytics | SAS Programming for R Users | Generative AI using SAS | Data Science with SAS Viya & Python | Responsible Innovation & AI Ethics
Get in touch
With a team of experienced instructors and a proven track record of success, we offer comprehensive coaching programs tailored to meet the diverse needs of our students