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Senior Statistical Advisor-Canada

  • Montréal, QC
  • On-site
  • Posted Sep 1, 2026
  • 1 position

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Employment type
Full-time
Experience level
Lead · 10+ years
Posting language
English
Working hours
40 hours per week

Job summary

The Senior Statistical Advisor provides statistical input for clinical trial development, including protocol design, sample size estimation, and data analysis. They also ensure all research activities comply with regulatory requirements and industry standards while collaborating with cross-functional teams.

Job details

The Senior Statistical Advisor provides statistical input for clinical trial development, including protocol design, sample size estimation, and data analysis. They also ensure all research activities comply with regulatory requirements and industry standards while collaborating with cross-functional teams. The role requires extensive experience in clinical trial statistics and the ability to communicate complex data to non-statisticians. Candidates must be proficient in reviewing statistical analysis plans and supporting scientific documentation for clinical study reports.

What you’ll do

The Senior Statistical Advisor provides statistical input for clinical trial development, including protocol design, sample size estimation, and data analysis. They also ensure all research activities comply with regulatory requirements and industry standards while collaborating with cross-functional teams.

Requirements

The role requires extensive experience in clinical trial statistics and the ability to communicate complex data to non-statisticians. Candidates must be proficient in reviewing statistical analysis plans and supporting scientific documentation for clinical study reports.

Benefits

  • Medical insurance
  • Dental insurance
  • Vision insurance
  • RRSP
  • Vacation
  • Personal days
  • Virtual medical clinic
  • Public transportation rebates
  • Social activities
  • Flexible work schedule

Listed skills

  • Regulatory Compliance · Preferred

Other relevant skills

Identified from the job description. Confirm important requirements above.

  • Clinical trial development
  • Protocol development
  • Statistical analysis
  • Sample size estimation
  • Power calculations
  • Randomization
  • Statistical methods
  • Data interpretation
  • Regulatory compliance
  • Clinical study reports
  • Scientific writing
  • Dermatology research

Job areas

  • Science & Research
  • Healthcare
  • Data & Analytics
  • Consulting

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