The Clinical SAS Course is official SAS training focused on managing clinical trial data, SAS programming, and reporting. It prepares learners to work on clinical research projects using globally accepted standards and tools.

The course is ideal for pharmacy, life sciences, biostatistics, and IT professionals who want to build expertise in clinical research and data programming. It is open to fresh graduates, students, statisticians, and working professionals seeking to transition into clinical research or clinical data programming.

Yes. Clinical SAS offers strong and growing career opportunities in pharma, CROs, and regulatory analytics. The demand for skilled programmers is high in India and globally, driven by the expansion of clinical research and regulatory requirements. It provides stable, long-term roles with clear growth paths.

It is the SAS Academy for Clinical Programming, the official SAS training program that prepares learners to work on clinical trials. The program covers SAS programming, CDISC standards (SDTM, ADaM), TLFs, data validation, and certification, aligning with global clinical research standards.

The course covers SAS programming, clinical data workflows, CDISC standards including SDTM and ADaM, creation of TLFs (Tables, Listings, Figures), data validation, and hands-on projects using real clinical trial datasets. Click here → to request latest syllabus.

Graduates are prepared for roles such as Clinical SAS Programmer, Statistical Programmer, and Clinical Data Analyst. They work with CROs, pharma companies, and regulatory analytics teams. The program also includes Talent Connect initiatives that link learners with hiring organizations.

You can submit your details here → and the SAS team will contact you with program details and next steps.

Clinical SAS stands for Clinical Statistical Analysis System. It refers to the use of SAS software for managing, analyzing, and reporting clinical trial data in the pharmaceutical, biotechnology, and healthcare industries. It involves applying SAS programming techniques to clinical research datasets to ensure accurate statistical analysis, generate regulatory-compliant reports, and support submissions to health authorities such as the US FDA and EMA.

Clinical SAS programmers play a key role in transforming raw clinical data into validated, analysis-ready datasets and outputs, which are critical for clinical trials, regulatory submissions, and drug approvals.

Clinical SAS focuses on programming, statistical analysis, and regulatory reporting using SAS software. Clinical SAS programmers work with clinical trial datasets to clean, transform, and analyze data, produce statistical outputs, and generate submission-ready reports for regulatory authorities such as the US FDA and EMA.

Clinical Data Management (CDM), on the other hand, centers on collecting, validating, and maintaining clinical trial data. CDM professionals are responsible for data entry, query management, database design, and ensuring data integrity throughout the trial process.

In short, Clinical SAS is more technical and analysis-focused, while Clinical Data Management is more operational and data-entry driven. Many professionals in CDM transition to Clinical SAS to specialize in programming and regulatory analytics.

Yes. The SAS Academy for Clinical Programming offers live online training accessible to all. Learners from Bengaluru, Mumbai, Chennai, Hyderabad, Pune, Ahmedabad, Delhi, and 15+ other cities across India, as well as from the USA, Canada, UK, Germany, Mexico, and Australia join the SAS Academy for Clinical Programming course every year.