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
- Valuable 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.

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