Senior Statistician

Adecco; Ottawa; On-site; CAD 95,000 - 110,000; Full time

Benefits offered by this job

Weekly pay

Health benefits

Training programs

Onboarding support

Job summary

Adecco is hiring a Senior Statistician for a full-time, clinical-research focused role in Ottawa, Ontario. The position emphasizes biostatistics, trial design, analysis, and regulatory support within medical device studies.

The candidate will design, analyze, and interpret clinical studies, collaborate with cross-functional teams, and ensure high-quality statistical reporting for regulatory submissions. Strong software proficiency is expected.

Qualifications

• Master's degree in Statistics, Biostatistics, Epidemiology, Mathematics or related field.
• Minimum 3 years of experience in biostatistics, clinical research, medical devices, or epidemiology.
• Experience developing analysis plans and clinical study reports.

Responsibilities

• Develop statistical methods sections for study protocols and analysis plans.
• Perform statistical analyses and interpret study results.
• Review reports for accuracy and regulatory compliance.
• Support regulatory submissions with statistical input.

Skills

Biostatistics

Clinical trial design

Statistical analysis

Epidemiology

Statistical programming

Education

Master's degree in Statistics/Biostatistics/Epidemiology

Tools

R

SAS

Minitab

Job description

Adecco is currently hiring a Senior Statistician for a full-time opportunity supporting clinical research and medical device studies. This role is ideal for professionals with experience in biostatistics, clinical trial design, statistical analysis, epidemiology, regulatory submissions, and statistical programming.

As a Senior Statistician, you will play a critical role in the design, analysis, interpretation, and reporting of clinical studies. You will collaborate with cross-functional teams to develop statistical methodologies, support regulatory submissions, and ensure the delivery of high-quality scientific data that supports business and clinical objectives.

• Pay Rate: $95000 to $110000/year
• Location: Ottawa, ON
• Job type: Temporary | Full-time
• Vacancy Status: This posting is for an existing vacancy.

Here’s why you should apply

• Paid weekly accurate and on time
• Strong health and safety programs
• Medical and dental benefits once qualified
• Free training programs
• New and quicker onboarding process

Responsibilities

Clinical Research & Statistical Analysis

• Develop statistical methods sections for clinical study protocols, analysis plans, and clinical study reports.
• Perform statistical analyses and interpret study results using appropriate methodologies.
• Review clinical reports to ensure accuracy, consistency, and compliance with reporting standards.
• Identify and resolve statistical, analytical, and reporting discrepancies.

Collaboration & Scientific Support

• Present statistical findings and recommendations to clinical, scientific, and cross-functional teams.
• Communicate statistical concepts to both technical and non-technical stakeholders.
• Serve as a statistical subject matter expert and support project teams throughout the study lifecycle.
• Contribute to the development of study designs and statistical approaches supporting regulatory submissions.

Compliance & Continuous Improvement

• Ensure statistical analyses comply with applicable regulatory and industry standards.
• Support a culture of quality, collaboration, and continuous improvement.
• Maintain accurate documentation and statistical records.
• Promote a safe and healthy work environment.

Qualifications and Skills

• Master's degree in Statistics, Biostatistics, Epidemiology, Mathematics, Engineering, or a related scientific discipline.
• Minimum of 3 years of experience in biostatistics, clinical research, medical devices, epidemiology, or related fields.
• Experience developing statistical analysis plans, protocol methodologies, and clinical study reports.
• Proficiency with statistical software such as R, SAS, Minitab, or similar platforms.
• Strong understanding of statistical modeling, study design, and data interpretation.
• Excellent verbal and written communication skills.
• Strong analytical thinking, problem-solving, and decision-making abilities.
• Ability to collaborate effectively with cross-functional stakeholders.
• Experience supporting regulatory submissions for medical devices is considered an asset.
• Knowledge of ICH-GCP, FDA regulations, and 510(k) submission processes is considered an asset.
• Must be legally eligible to work, and reside in Canada

At Adecco our purpose is simple: to make the future work for everyone. We live our values, Passion, Collaboration, Inclusion, Courage, and Customers at Heart, by fostering a workplace where diversity is celebrated and every voice matters. We encourage applications from individuals of all backgrounds and identities. Together, we're making the future work for everyone.