Clinical SAS Programmer / Senior Clinical SAS Programmer Experience: 5 Years Mandatory Skills: Clinical SAS Programming CDISC Standards (SDTM, ADaM) Strong hands-on ADaM Programming TLF Development & Validation Safety and Efficacy Programming SAS Macro Programming Define.xml and Pinnacle 21 Independent/Scratch Programming End-to-End Clinical Trial Experience (Phase II/III) Preferred Skills: Oncology, Neurology, or Immunology studies Regulatory Submission Support Reviewer/Lead experience Robust knowledge of derivations, imputations, and analysis datasets Key Responsibilities: Develop and validate SDTM and ADaM datasets. Create and validate TLFs for clinical studies. Support efficacy and safety analyses. Perform independent SAS programming and validation. Ensure compliance with CDISC standards and regulatory requirements.