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 strong 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