Senior Biostatistician

Everest Clinical Research Services Inc; Toronto; Remote; CAD 85,000 - 120,000; Full time

Job summary

Everest Clinical Research is looking for a Senior Biostatistician to manage statistical operations and contribute to clinical trials. This role offers remote work options across Canada and emphasizes strong leadership, statistical expertise, and commitment to quality. Candidates with a Ph.D. or a Master’s degree and relevant experience are encouraged to apply.

Qualifications

• Ph.D. required or Master's with relevant experience.
• 2+ years experience for Ph.D. candidates; 4+ years for Master's.
• Strong performance history needed.

Responsibilities

• Lead statistical and programming operations and improve efficiency.
• Provide expertise in design, analysis, and reporting of clinical trials.
• Conduct statistical analyses and validate results.

Skills

Leadership

Statistical Programming

Data Quality

Project Management

Education

Ph.D. in statistical science or related field

Master’s degree

Job description

Everest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to pharmaceutical, biotechnology, and medical device industries worldwide. We serve well-known companies and work with advanced drugs, biologics, and medical devices in development.

Founded in 2004, Everest has a strong foundation as a statistical and data management center of excellence. Our headquarters are in Markham, Ontario, Canada, with additional sites in Bridgewater (New York area), New Jersey, Shanghai, and Taipei.

Known for high-quality deliverables, superior customer service, and flexibility, Everest continues to grow dynamically, driven by a commitment to quality, customer-focus, and flexibility.

We are seeking dedicated, skilled, and customer-focused individuals to join our team as Senior Biostatisticians, based in Markham, Ontario, or remotely across Canada in accordance with our Work from Home policy.

Key Responsibilities:

1. Leadership and Project Management: Lead daily work issues, improve efficiency, and manage statistical and programming operations; oversee project delivery, ensuring quality and timeliness, and foster client trust.
2. Statistical Planning and Methodologies: Provide expertise in design, analysis, and reporting of clinical trials; contribute to protocol writing, sample size calculation, randomization specifications, and develop SAPs.
3. Statistical Programming: Develop/review dataset specifications, perform QC validation, lead statistical dry runs, and ensure data quality and standards compliance.
4. Analysis and Reporting: Conduct statistical analyses, validate results, contribute to CSR and publication materials, and support dissemination activities.
5. Data Collection and Cleaning Support: Provide statistical input on data collection tools, review data management plans, and assist in database lock preparations.

Additional responsibilities include training, policy compliance, proper archiving, and professional development.

Qualifications and Experience: Ph.D. in statistical science or related field with 2+ years of relevant experience, or Master’s degree with 4+ years of relevant experience, demonstrating sustained high performance.