Role & responsibilities
Develop, validate, and maintain clinical trial datasets using Base SAS, SAS Macros, and SAS SQL.
Generate highly accurate TLFs (Tables, Listings, and Figures) to support Clinical Study Reports (CSR) and biostatistics teams.
Ensure strict compliance with CDISC standards, specifically focusing on the creation and validation of SDTM and ADaM datasets.
Perform ETL (Extract, Transform, Load) activities on raw clinical data imported from various EDC (Electronic Data Capture) platforms.
Write and execute code to generate Edit Checks, resolve data discrepancies, and implement robust data quality control procedures.
Utilize SAS ODS and procedures like Proc SQL, Proc Freq, and Proc Means for custom reporting.




Maintain compliance with regulatory guidelines including ICH, GCP, and FDA 21 CFR Part 11.

Preferred candidate profile
Masters degree in Bioinformatics, Biotechnology, Pharmacy (M.Pharm), or Life Sciences.
Basic understanding or certification in Clinical SAS Programming. Familiarity with R Programming or Python is a robust advantage.
Solid analytical mindset with a keen interest in Clinical Data Management (CDM).
Excellent problem-solving skills and the ability to work collaboratively in cross-functional clinical trial teams.

📌 Clinical Sas Programmer Bengaluru
🏢 Airvin Skills
📍 Bengaluru