Senior Statistical Advisor
- Canada
Full-time
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Job details
- Job type
- Full-time
- Posting language
- English
- Posted
Original job description
This position is listed on behalf of a partner company, which manages all applications and next steps. Our partner is looking for a Senior Statistical Advisor based in Canada.
The Senior Statistical Advisor plays a key role in shaping the statistical strategy and methodology behind Phase I–IV clinical trials. You will provide expert statistical guidance throughout clinical development, from protocol design and sample size calculations to data analysis and interpretation. Working closely with clinical research teams, scientific writers, and external sponsors, you will help ensure that studies generate reliable, meaningful, and scientifically robust results. Your expertise will contribute to the development of efficient, cost-effective clinical trials and support the preparation of high-quality regulatory submissions. You will also help strengthen statistical standards, improve internal processes, and ensure compliance with applicable regulations and industry guidelines. This position offers the opportunity to apply advanced statistical knowledge in a collaborative clinical research environment focused on scientific quality and sponsor satisfaction. It is an excellent opportunity for a statistics professional seeking to make a meaningful impact on clinical research and drug development.
How Jobgether Works
We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team.
We appreciate your interest and wish you the best!
Why Apply Through Jobgether?
Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
The Senior Statistical Advisor plays a key role in shaping the statistical strategy and methodology behind Phase I–IV clinical trials. You will provide expert statistical guidance throughout clinical development, from protocol design and sample size calculations to data analysis and interpretation. Working closely with clinical research teams, scientific writers, and external sponsors, you will help ensure that studies generate reliable, meaningful, and scientifically robust results. Your expertise will contribute to the development of efficient, cost-effective clinical trials and support the preparation of high-quality regulatory submissions. You will also help strengthen statistical standards, improve internal processes, and ensure compliance with applicable regulations and industry guidelines. This position offers the opportunity to apply advanced statistical knowledge in a collaborative clinical research environment focused on scientific quality and sponsor satisfaction. It is an excellent opportunity for a statistics professional seeking to make a meaningful impact on clinical research and drug development.
How Jobgether Works
We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team.
We appreciate your interest and wish you the best!
Why Apply Through Jobgether?
Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
More about this job
Responsibilities
Shape statistical strategy and methodology for Phase I–IV clinical trials, providing guidance on protocol design, sample size calculations, data analysis, and interpretation. Collaborate with clinical research teams, scientific writers, and sponsors to support robust studies and regulatory submissions, strengthen statistical standards, and improve internal processes.
Requirements
The posting does not specify formal education, years of experience, or other explicit qualifications. It indicates a need for advanced statistical expertise in clinical trials, including study design, analysis, interpretation, and regulatory compliance.
Skills
- Statistical Strategy
- Clinical Trial Design
- Statistical Methodology
- Sample Size Calculations
- Clinical Data Analysis
- Data Interpretation
- Clinical Development
- Regulatory Submissions
- Statistical Standards
- Regulatory Compliance
- Clinical Research
Visa sponsorship
Not detected in the job text
Categories
- Science & Research
- Healthcare
- Data & Analytics
Keywords
- Phase I–IV Clinical Trials
- Statistical Strategy
- Statistical Methodology
- Protocol Design
- Sample Size Calculations
- Clinical Development
- Data Analysis
- Data Interpretation
- Clinical Research
- Scientific Writing
- External Sponsors
- Regulatory Submissions
- Statistical Standards
- Regulatory Compliance
- Industry Guidelines
- Clinical Trial Efficiency
- Drug Development