Clinical Sas Programmer

Key Responsibilities

• Develop and validate SDTM and ADaM datasets according to CDISC standards.
• Generate Tables, Listings, and Figures (TLFs) for clinical study reports.
• Perform data cleaning, validation, and quality control checks.
• Write and optimize SAS programs using DATA steps, PROC SQL, and Macros.
• Prepare and review Define.xml and submission-ready datasets.
• Support regulatory submissions (FDA, EMA).
• Collaborate with Biostatistics, Data Management, and Clinical teams.
• Ensure compliance with GCP and industry standards.
• Document programming specifications, validation reports, and workflows.