Join Cytel as a Senior Biostatistician and lead impactful clinical trials for a major pharmaceutical client. Apply your statistical expertise to support cutting-edge treatments through all phases of trials.
This role is perfect for an experienced biostatistician with a passion for clinical analysis and a cooperative spirit. You’ll be integral in developing study protocols and leading statistical analyses while ensuring adherence to regulatory standards. With over five years in clinical trials, your contributions will be crucial in pushing clinical development forward.
Key Responsibilities:
• Lead statistical analysis for clinical studies
• Create and review study protocols and sample size estimates
• Develop and maintain statistical analysis plans (SAPs)




• Compile integrated summaries for regulatory submissions
• Engage with internal teams and external partners effectively
Requirements:
• Master’s degree in statistics; Ph.D. highly sought
• 5+ years of experience in the pharmaceutical industry
• Proficient in SAS programming; familiarity with R is advantageous
• Solid knowledge of CDISC compliance for submissions
• Solid communication skills for effective collaboration
Utilize your biostatistical skills to mentor teams and ensure the quality of clinical advancements at Cytel.
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📌 Cytel Senior Biostatistician In Pharma Toronto
🏢 Cytel
📍 Toronto