Qtech-Sol Professional Development Center

Live Webinar — Free Registration

Clinical SAS Programmer (CDAR)

Become industry-ready in Analytics & Reporting: data extraction & transformation, Base & Advanced SAS, Macros & SQL, QC, CDISC standards, and generating TLFs for regulatory submissions — with live Q&A.

Webinar Snapshot

Date

Tue, Feb 3, 2026;

Duration

60 minutes

Level

Beginner–Intermediate

Mode

Live Online (Google Meet)

Seats

Limited (first-come, first-served)

Certificate

Attendance Certificate

Webinar Preview

What You’ll Learn

Data extraction & transformation; SAS programming & scripting
Data validation, cleaning, and quality control; handling discrepancies/errors
Base SAS fundamentals (processing, merging, sorting, transposing)
Advanced SAS: macro programming, SQL within SAS, efficiency programming
Reporting & statistical outputs: TLFs; key statistical procedures
Regulatory compliance & documentation; CDISC (SDTM/ADaM)

Why Attend?

Free registration with certificate
Direct pathway to CDAR training enrollment
Access to Resume Marketing Services (RMS)
Insights into industry-aligned A&R practices
Networking and interactive Q&A with experts

Webinar Agenda (60 mins)

00:00–00:05

Welcome & outcomes

00:05–00:15

SAS fundamentals: Base, data manipulation & validation

00:15–00:30

Macro & SQL programming; efficiency & error handling

00:30–00:45

Statistical procedures & report generation (TLFs)

00:45–00:55

Regulatory compliance, CDISC & documentation best practices

00:55–01:00

Q&A + next steps

Aligned to ICH-GCP, CDISC, FDA/EMA guidelines. Real-data SAS projects included.

[USA]

“Clear walk-through of Base SAS and TLF generation. I built my first listings in a week.”

— Taylor S., Raleigh, USA

[Canada]

“Macros + SQL tips were practical. I now document and QC my outputs correctly.”

— Priya K., Montreal, Canada

[India]

“CDISC mapping examples finally made SDTM/ADaM click for me.”

— Arjun R., Pune, India

Application Form

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Accepted: PDF, DOC/DOCX, TXT, RTF, images, XLS/XLSX

You’ll receive confirmation and the joining link via email after submission.

front- Book 1-on-1 Call Download Program Catalog

Meet the Instructor

Dr. Chandra Nate, PhD

Clinical Analytics & Reporting Expert · 25+ years in the Pharmaceutical Industry

Dr. Nate is a seasoned leader in Clinical Operations, Analytics & Reporting, and Clinical Technology systems. With hands-on expertise in SAS Programming, CDISC (SDTM/ADaM), EDC/CDMS, Data Quality, and Regulatory Compliance, he has trained and mentored hundreds of professionals globally. Known for bridging programming with statistical reporting, Dr. Nate focuses on job-ready workflows you can apply immediately in A&R roles.

Learning Outcomes

Write effective SAS programs for clinical trial datasets
Clean, transform & manipulate raw clinical data accurately
Apply SAS Macros & SQL to optimize programming tasks
Generate TLFs (Tables, Listings, Figures) for submissions
Perform statistical analyses per protocol & regulatory needs
Implement CDISC standards (SDTM, ADaM) in programming
Ensure compliance with SOPs & global regulations
Maintain proper documentation & version control practices
Support statisticians & clinical teams in data reporting