Senior Biostatistician — Remote or On-site (Toronto)

Everest Clinical Research Services Inc; Markham; Hybride; CAD 150 000 - 200 000; Plein temps

Avantages offerts par ce poste

Med/Dental/Vision

Pension plan

Paid time off

Bonus potential

Résumé du poste

Everest Clinical Research Services Inc. is seeking a Principal Biostatistician for the Toronto/Markham, Ontario, Canada location with remote work options within Canada. The role requires leading statistical strategies across drug development programs and mentoring a team of biostatisticians and programmers.

The ideal candidate holds a Ph.D. or Master’s with extensive experience, and will contribute to protocol design, SAP development, and regulatory submissions while ensuring high-quality

Qualifications

• A Ph.D. degree in statistical science, mathematical analysis or related fields with at least 7 years of relevant experience
• OR a Master’s degree in the above fields with at least 10 years of relevant experience, with demonstrated exceptional ability and performance.

Responsabilités

• Provide statistical oversight on trials and lead statistical design, analysis planning and reporting.
• Coach and mentor junior statisticians and programmers on project deliverables.
• Write SAPs, trial protocols, and reports; ensure regulatory compliance and quality control.
• Review ADaM datasets and data management outputs for accuracy and completeness.
• Consult with medical teams and contribute to publications, abstracts and posters.
• Interact with regulatory agencies as a statistical liaison to support submissions.

Formation

Ph.D. in statistical science

Master’s degree in statistics or related field

Description du poste

Everest Clinical Research Services Inc. is seeking a Principal Biostatistician for the Toronto/Markham, Ontario, Canada location with remote work options within Canada. The role requires leading statistical strategies across drug development programs and mentoring a team of biostatisticians and programmers.

The ideal candidate holds a Ph.D. or Master’s with extensive experience, and will contribute to protocol design, SAP development, and regulatory submissions while ensuring high-quality