Clinical SAS Programmer / Senior Programmer (2–5 Years)

Job Description

The Clinical SAS Programmer independently handles programming activities for clinical studies, ensuring high-quality, submission-ready datasets and statistical outputs.

Key Responsibilities

• Develop SDTM, ADaM, and analysis datasets

• Create and validate TLFs as per SAP

• Perform independent programming and QC

• Support regulatory submissions (FDA, EMA)

• Collaborate with Biostatistics and Data Management teams

• Maintain programming documentation and standards

Skills & Requirements

• 2–5 years of Clinical SAS programming experience

• Strong hands-on experience with SDTM, ADaM, and TLFs

• Knowledge of CDISC, ICH-GCP, and regulatory guidelines

• Experience in validation and submission support