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Toronto, ON · Science/Research

Our client requires a Biostatistician to join a global team of experts and work with some of the world’s most prestigious pharmaceutical and life sciences businesses.
Biostatistician I, Biostatistician II
Biometrics, Health Economics & Outcomes
The Biostatistician is responsible for intermediate-level statistical analyses and programming for clinical trials and/or research projects. The Biostatistician will provide a wide range of advanced statistical expertise, guidance, and support to internal and external clients. This position will assist in trial design, the development of statistical analysis plans and data management review and consultation.

What’s in it for you?
No commute, no parking, an extra hour’s sleep!
A knowledgeable, high achieving, experienced and diverse team
An international and inclusive atmosphere
Exciting career trajectory: Biostatistician Biostatistician II Senior Biostatistician Principal Biostatistician Manager

Duties and Responsibilities
  • Research and development of statistical methodologies.
  • Investigate and implement innovative technologies, processes, and procedures.
  • Participate in developing and executing marketing strategies and plans for new and existing clients
  • Participate in developing and executing customer relationship management plans.
  • Participate in business development and maintenance activities.
  • Oversee data management and programming activities for assigned projects. Serve as primary contact between medical/clinical and data management in data related issues.
  • Provide statistical and data management input into protocol development. Write Statistical Analysis Plans for assigned projects. Oversee IVRS and web-based patient randomization processes for assigned projects.
  • Oversee the development of Data Management Plans (DMPs) for assigned projects.
  • Provide statistical input into Case Report Forms (CRF) design for assigned projects, and oversee efforts in developing, reviewing, and testing of the CRFs.
  • Participate in Study Manual Development, and in clinical trial initiation meetings such as investigator meetings, site monitor/coordinator training sessions.
  • Oversee programming support activities for assigned projects. Validate the accuracy, consistency and integrity of the statistical output displays generated by the Study Programmer.

Minimum Requirements
  • Ph.D. degree or equivalent in statistical science, mathematical analysis, or related field plus 1 - 2 years relevant experience directly related to the duties and responsibilities specified OR Master’s degree plus 4 - 5 years relevant experience directly related to the duties and responsibilities specified.
  • Completed degree(s) from an accredited institution that are above the minimum education requirement may be substituted for experience on a year for year basis.


Thank you for your interest in this job posting.

We look forward to hearing from you.

TalentSphere Staffing Solutions


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