Senior Statistical Advisor

📋 Description

• Provide statistical expertise for Phase I–IV clinical trials, including protocol development, trial
• Review statistical analysis plans and validate statistical outputs to ensure accuracy, consistency
• Communicate with sponsors and clients regarding study protocols, statistical methodologies
• Contribute statistical expertise to clinical development activities and regulatory submissions
• Support scientific writers in preparing Clinical Study Reports by reviewing statistical results
• Advise on the design of valid, efficient, and cost-effective clinical trials and other research

🎯 Requirements

• A strong academic background in statistics, biostatistics, or a related quantitative discipline is
• Experience or demonstrated expertise in clinical trial methodology, particularly across Phase I–IV
• Ability to critically review statistical analysis plans, validate statistical outputs, interpret
• Understanding of applicable clinical research regulations, industry guidelines, and Good Clinical
• Strong written and verbal communication skills, including the ability to explain complex
• Excellent attention to detail, sound scientific judgment, and the ability to recommend appropriate

🎁 Benefits

• Permanent, full-time position.
• Flexible work schedule to support work-life balance.
• Comprehensive health coverage: medical, dental, and vision benefits.
• Retirement planning: Registered Retirement Savings Plan (RRSP).
• Time off: vacation allowance and personal days.
• Additional perks: access to a virtual medical clinic, public transportation rebates, and social