Lead SAS Programmer Clinical Trials (Ontario)

Lead SAS Programmer Clinical Trials (Ontario)

09 Nov
|
Alira Health Canada
|
Ontario

09 Nov

Alira Health Canada

Ontario

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.

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

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