Senior Statistician

Job summary

The Senior Statistician will develop statistical methodologies for clinical study protocols and perform complex analyses to interpret study results. They will also collaborate with cross-functional teams to support regulatory submissions and ensure high-quality scientific data reporting.

Job details

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 Are you interested in this position? Apply now! Our dynamic team of recruiters will reach out if you qualify for this role. 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. Please reach out to learn how the Aspire Academy can upskill you into your next role. @@j #CAAP1956

What you’ll do

The Senior Statistician will develop statistical methodologies for clinical study protocols and perform complex analyses to interpret study results. They will also collaborate with cross-functional teams to support regulatory submissions and ensure high-quality scientific data reporting.

Requirements

Candidates must hold a Master's degree in a relevant scientific discipline and possess at least 3 years of experience in biostatistics or clinical research. Proficiency in statistical software and a strong understanding of study design and regulatory standards are essential.

Benefits

• Paid weekly • Health and safety programs • Medical benefits • Dental benefits • Free training programs

Listed skills

• Problem solving · Preferred
• Communication Skills · Preferred

Other relevant skills

Identified from the job description. Confirm important requirements above.

• Biostatistics
• Clinical trial design
• Statistical analysis
• Epidemiology
• Regulatory submissions
• Statistical programming
• R
• SAS
• Minitab
• Statistical modeling
• Data interpretation
• Analytical thinking
• Problem-solving
• Communication skills
• ICH-GCP
• FDA regulations

Job areas

• Science & Research
• Healthcare
• Data & Analytics
• Technology