Lead SAS Programmer Clinical Trials (Toronto)

Lead SAS Programmer Clinical Trials (Toronto)

08 Nov
|
Alira Health Canada
|
Toronto

08 Nov

Alira Health Canada

Toronto

SAS programming and clinical research expertise define this Principal Statistical Programmer role with Alira Health. Support high-quality deliverables across client projects.

This position leads statistical programming activities, including complex clinical projects, while following standard operating procedures and agreed timelines. Responsibilities include CDISC dataset development, statistical analysis results, risk support, resource deployment, audits, and mentoring. Knowledge of R is a plus.

Key Responsibilities:

- Specify, program, and validate clinical study datasets
- Program statistical analysis results, tables, listings, and figures
- Identify scope changes and risks to contractual delivery
- Report deviations, KPIs, complaints, and manage CAPAs




- Support audits, training, and effective departmental maintenance

Requirements:

- At least five years in statistical programming
- Excellent SAS programming skills and R knowledge preferred
- Degree or equivalent experience in relevant quantitative discipline
- Robust clinical research principles and techniques knowledge
- Analytical problem-solving and effective prioritization abilities

Use SAS, clinical research knowledge, CDISC programming, and analytical judgment to deliver validated clinical project outputs.

📌 Lead SAS Programmer Clinical Trials (Toronto)
🏢 Alira Health Canada
📍 Toronto

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