Unlock new career potential as a Senior Biostatistician with Cytel, dedicated to a global pharmaceutical client. Utilize your advanced statistical skills to influence the next generation of clinical treatments. In this role, you will leverage your expertise in biostatistics to conduct thorough analyses and support Phase I-IV clinical studies.

Your experience will guide the creation of study protocols and statistical analysis plans, ensuring compliance with regulatory guidelines. This is an opportunity to blend technical skills with project leadership in a team-oriented setting. Key Responsibilities:

- Provide expertise in statistical methods for clinical research
- Participate in protocol development and sample size strategy




- Design and execute statistical analysis plans (SAPs)
- Produce clinical reports and integrated submissions
- Collaborate across various clinical and regulatory functions Requirements:
- Master’s degree in statistics or related; Ph.D. recommended
- Minimum 5 years of clinical trial experience
- Proficiency in SAS; R programming knowledge preferred
- Understanding of CDISC requirements for submissions
- Excellent ability to communicate complex methodology Enhance your role in clinical development at Cytel and make a difference in patient care.

📌 Experienced Biostatistician in Clinical Development (Toronto)
🏢 Cytel
📍 Toronto