Lead SAS Programmer Clinical Trials (Winnipeg)

Lead SAS Programmer Clinical Trials (Winnipeg)

09 Nov
|
Alira Health Canada
|
Winnipeg

09 Nov

Alira Health Canada

Winnipeg

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

Solid 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 (Winnipeg)
🏢 Alira Health Canada
📍 Winnipeg

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