Lead clinical trial programming with SAS, CDISC, SDTM, and ADaM expertise in oncology statistical programming. Prepare submission-ready data and outputs.
This senior statistical programmer supports all statistical programming activities for clinical data. The work includes conversions, analysis datasets, study TFLs, and programming specifications. You will also contribute to best practices, implementation guides, and customer requirements.
Key Responsibilities: Prepare clinical data for submission using CDISC or customized standards
Develop SAS programs for conversions and analysis datasets
Program study TFLs from SAPs and shells
Review data conversions, datasets, outputs, and programming
Create programming specifications for SDTM, ADaM, and derived data
Requirements: Bachelor’s degree in statistics, computer, or life science
Minimum eight years programming on clinical trials
Positive knowledge of TFL programming
Experience with CDISC SDTM and ADaM standards
Experience preparing Reviewer’s Guide and Define.xml documents
Apply senior SAS programming expertise to oncology clinical trials, CDISC standards, TFLs, and submission-focused statistical programming.

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📌 Senior Oncology Statistical Programmer SAS (Ontario)
🏢 Connect Life Sciences
📍 Ontario