Clinical SAS Programmer / Senior Clinical SAS Programmer
Experience: 5+ Years
Mandatory Skills:
Clinical SAS Programming
CDISC Standards (SDTM, ADaM)
Robust 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
Solid 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.