Principal Statistician

Warman O'Brien; Canada; Remote; CAD 80,000 - 120,000; Full time

Job summary

Join a globally recognized pharmaceutical company as a Principal Biostatistician, where your statistical insights will drive the development of life-changing therapies. In this remote-friendly role, you'll lead impactful clinical programs, mentor a team of biostatisticians, and collaborate with multidisciplinary teams to innovate drug development protocols. Your expertise in statistical analysis and project management will be key in ensuring compliance with regulatory guidelines and delivering high-quality results. This is an exciting opportunity to advance your career in a supportive environment that values collaboration and innovation.

Qualifications

• Advanced degree in Statistics with significant experience in the field.
• Strong proficiency in statistical analysis and regulatory requirements.

Responsibilities

• Oversee clinical trial programs and ensure rigorous statistical practices.
• Mentor biostatisticians and develop collaborative team dynamics.

Skills

Statistical Analysis

Programming

Project Management

Leadership

Education

Ph.D. in Statistics

Master’s in Statistics

Job description

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Become a key member of a globally recognized Pharmaceutical company, where your statistical insights will power the development of life-changing therapies. We're looking for a driven Principal Biostatistician to lead impactful clinical programs and advance your career in a supportive, remote-friendly environment.

What will you be doing?

• Oversee clinical trial programs, driving operational efficiency and ensuring rigorous statistical practices.
• Mentor and develop biostatisticians and programmers, fostering a collaborative and growth-oriented team.
• Collaborate with multidisciplinary teams to design innovative protocols and contribute to strategic drug development decisions.
• Develop and implement Statistical Analysis Plans (SAPs), conduct complex statistical modelling, and ensure high-quality deliverables.
• Maintain compliance with regulatory guidelines, manage statistical quality control, and support regulatory interactions.

What do you bring to the table?

• Advanced degree (Ph.D. or Master’s) in Statistics or related field with significant experience (7+ years Ph.D., 10+ years Master’s).
• Strong proficiency in statistical analysis, programming, and regulatory requirements.
• Proven leadership abilities, project management skills, and strategic thinking.
• Desire to work in a collaborative and innovative remote environment.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Analyst, Science, and Research

• Industries

  Pharmaceutical Manufacturing, Biotechnology Research, and Medical Equipment Manufacturing

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