Clinical SAS Programmer / Senior Clinical SAS Programmer
Experience: 2-6 Years
Mandatory Skills
Clinical SAS Programming CDISC Standards (SDTM, ADa M) Strong hands-on ADa M 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 Solid knowledge of derivations, imputations, and analysis datasets Key Responsibilities:
Develop and validate SDTM and ADa M 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.