Clinical SAS Programmer / Senior Clinical SAS Programmer
Experience: 2-6 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.