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Non-Clinical Statistician - VIE Contract - Job Opportunity at Sanofi

Toronto, Canada
Contract
Entry-level
Posted: July 1, 2025
On-site
CAD 65,000 - 80,000 annually. This estimate reflects entry-level pharmaceutical statistician compensation in Toronto's competitive market, with the VIE program structure potentially offering additional international mobility benefits that enhance total compensation value.

Benefits

Access to Sanofi's global iMove program providing international career development opportunities across 40+ countries, significantly enhancing professional mobility and cross-cultural competence
Mentoring and guidance from inspirational senior leaders in pharmaceutical statistics, accelerating professional development through structured knowledge transfer
Direct exposure to cutting-edge vaccine research and development processes, positioning candidates at the forefront of global healthcare innovation
Opportunity to impact millions of patients worldwide through statistical contributions to vaccine development and manufacturing optimization
Integration into a multicultural work environment fostering global perspective and collaborative skills essential for international pharmaceutical careers

Key Responsibilities

Drive statistical excellence in vaccine research, development, and manufacturing by collaborating directly with scientists and senior statisticians in Chemistry, Manufacturing, and Controls (CMC), ensuring robust analytical foundations for life-saving vaccine production
Provide critical statistical support for biological assay and analytical method development across pre-clinical and clinical R&D phases, directly influencing the success and timeline of vaccine development programs
Deliver specialized statistical expertise to analytical science and CMC/QC operations for vaccines and biologics, ensuring compliance with regulatory standards and optimization of manufacturing processes
Challenge and optimize experimental designs in collaboration with senior statisticians, demonstrating analytical thinking and contributing to more efficient and scientifically sound research methodologies
Develop and implement appropriate statistical methodologies following internal procedures, building expertise in pharmaceutical-specific analytical approaches while maintaining regulatory compliance
Ensure comprehensive follow-up and traceability of statistical analyses including planning, prioritization, and reporting, maintaining the high documentation standards critical for regulatory submissions
Translate complex statistical conclusions into actionable insights for scientific teams, bridging the gap between mathematical analysis and practical research applications
Provide statistical consulting and training to scientists on demand, establishing expertise as a trusted advisor and contributing to organizational statistical literacy

Requirements

Education

Master degree or Ph.D in statistics or related field

Experience

1 year of professional experience after graduation would be a plus

Required Skills

Ability to work in a multi-cultural environment Ability to work autonomously Ability to work in the team Eager to learn and open-minded Good communication skills Creative mindset and problem-solving skills Very good sense of organization and time management Knowledge of R Knowledge of SAS (Statistical Analysis System) and JMP would be a plus Fluent English (written and verbal)
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Sauge AI Market Intelligence

Industry Trends

The pharmaceutical industry is experiencing unprecedented demand for statistical expertise in vaccine development, driven by recent global health events and the accelerated timeline requirements for new vaccine approvals. This has created a specialized niche for non-clinical statisticians who can bridge laboratory research and regulatory compliance. Digital transformation in pharmaceutical R&D is driving increased adoption of advanced statistical software platforms like R, SAS, and JMP, with companies seeking statisticians who can leverage these tools for more sophisticated analytical approaches in biologics manufacturing and quality control. Regulatory agencies worldwide are implementing more stringent statistical requirements for vaccine approval processes, creating sustained demand for statisticians with expertise in biological assay validation and analytical method development specifically within the CMC framework.

Role Significance

Typically embedded within a team of 5-8 statisticians and data scientists, working closely with 10-15 research scientists and laboratory personnel, with regular interaction with senior statisticians and cross-functional CMC teams.
This is an entry-level professional role with significant growth potential, positioned as a bridge between academic statistical training and senior pharmaceutical statistician responsibilities. The role offers substantial learning opportunities while contributing meaningfully to vaccine development processes.

Key Projects

Statistical validation of biological assays for vaccine potency and safety testing, ensuring reliable measurement methods for regulatory submissions Development of statistical models for manufacturing process optimization, contributing to improved vaccine production efficiency and consistency Analysis of pre-clinical and clinical trial data to support vaccine development decisions and regulatory filing strategies Implementation of quality control statistical methods for ongoing vaccine manufacturing operations

Success Factors

Developing deep expertise in pharmaceutical-specific statistical applications, particularly biological assay validation and CMC statistical methods, which are highly specialized and valuable skill sets in the industry Building strong collaborative relationships with multidisciplinary scientific teams while maintaining statistical rigor and independence in analytical recommendations Mastering regulatory statistical requirements and documentation standards, which are critical for vaccine approval processes and long-term career advancement in pharmaceutical statistics Cultivating both technical statistical skills and business acumen to translate analytical insights into actionable recommendations for research and manufacturing teams

Market Demand

High demand driven by pharmaceutical industry expansion, regulatory complexity, and the critical role of statistical analysis in vaccine development and manufacturing quality assurance.

Important Skills

Critical Skills

Proficiency in R programming is essential as it has become the primary statistical computing platform for pharmaceutical research, with regulatory agencies increasingly accepting R-based analyses for submission packages. The open-source nature and extensive package ecosystem make R indispensable for modern pharmaceutical statistics. Strong communication skills are crucial for translating complex statistical concepts to diverse scientific audiences, a capability that distinguishes successful pharmaceutical statisticians and directly impacts project success and career advancement opportunities. Multicultural collaboration abilities are particularly valuable in global pharmaceutical companies like Sanofi, where projects span multiple countries and regulatory jurisdictions, requiring effective cross-cultural communication and adaptability.

Beneficial Skills

SAS expertise, while listed as a plus, remains highly valuable in pharmaceutical statistics due to its strong regulatory acceptance and widespread use in clinical trials and manufacturing quality control systems JMP knowledge provides competitive advantage for exploratory data analysis and visualization, particularly useful for communicating statistical insights to non-statistician stakeholders in research and manufacturing teams Understanding of regulatory statistical guidelines and pharmaceutical development processes would significantly accelerate onboarding and effectiveness in the specialized pharmaceutical statistics environment

Unique Aspects

The VIE (Volontariat International en Entreprise) program structure provides exceptional international mobility opportunities rare in early-career pharmaceutical positions, with potential for global assignments across Sanofi's 40+ country presence
Direct involvement in vaccine development and manufacturing statistics offers exposure to one of the most impactful and rapidly evolving areas of pharmaceutical science, particularly relevant given recent global health priorities
Integration into Sanofi's Digital Data & Technology team positions the role at the intersection of traditional pharmaceutical statistics and emerging data science applications
The specific focus on CMC (Chemistry, Manufacturing, and Controls) statistics provides specialized expertise that is highly valued and relatively scarce in the pharmaceutical job market

Career Growth

Progression to senior roles typically occurs within 3-5 years with demonstrated expertise in pharmaceutical statistics and successful project delivery, with management opportunities emerging after 5-7 years of specialized experience.

Potential Next Roles

Senior Non-Clinical Statistician with expanded responsibility for statistical methodology development and junior staff mentoring Principal Statistician specializing in vaccine CMC or clinical development with strategic input on program design Statistical Manager overseeing multiple projects and statistician teams within pharmaceutical development Regulatory Affairs Statistician focusing on submission strategy and agency interactions

Company Overview

Sanofi

Sanofi stands as one of the world's largest pharmaceutical companies with a particularly strong position in vaccines, delivering over 500 million vaccine doses annually and maintaining significant market presence across therapeutic areas. The company's commitment to R&D innovation and global health initiatives positions it as a leader in pharmaceutical development.

Sanofi ranks among the top 5 global pharmaceutical companies by revenue, with particularly strong market leadership in vaccines and specialty medicines, providing employees with exposure to industry-leading practices and cutting-edge research initiatives.
Toronto represents a strategic location for Sanofi's North American operations, serving as a key hub for R&D activities with access to Canada's strong pharmaceutical talent pipeline and supportive regulatory environment for clinical research.
Sanofi emphasizes collaborative international culture with strong focus on employee development and cross-functional teamwork, particularly evident in programs like iMove that prioritize global mobility and diverse experience acquisition.
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