Senior Manager Biostatistician Consultant Remote in Canada - 24 months contract

Posted 3 Days Ago
Be an Early Applicant
Hiring Remotely in Canada
Remote
120-150 Annually
Senior level
Pharmaceutical
The Role
The Senior Manager Biostatistician Consultant is responsible for protocol design, statistical analysis, and supporting submission activities for clinical trials while leading project deliverables.
Summary Generated by Built In

Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds….

ClinChoice is searching for an Senior Manager Biostatistician Consultant to join one of our clients.

ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client’s counterparts.  


Job Duties

This position is responsible for working with study team members and the project statistician to contribute to design of early/late-stage protocols across multiple therapeutic areas, help draft protocols or amendments, develop and write statistical analysis plans, and perform statistical analyses for interim and final reports to be submitted to regulatory agencies.

The position will also support submission activities, including design, analysis and reporting of integrated summaries for safety and efficacy.

Attendance and statistical contributions at study team meetings are expected.

Within the BDM Department, leadership skills are needed to contribute to the organization and scheduling of study deliverables in collaboration with Statistical Programmers and Data Managers.  

Qualification and Required Skills 

  • MS or PhD in Statistics or Biostatistics
  • PhD +4 years (or MS +9 years) clinical trial experience in either a biotechnology or pharmaceutical company
  • Hands-on Phase I/II/III clinical trial experience and proficient in SAS programming. Excellence in R programming desirable.
  • Excellent oral and written communication skills.
  • Although not required, previous experience with regulatory submissions in the US, Europe, Japan, and Rest of the World, is desirable.


Open Date: 5/14/2026

Close Date: 6/3/2026


ClinChoice Canada Inc. is proud to be an equal opportunity employer, valuing and respecting diversity.  We are committed to inclusive, barrier-free recruitment and selection processes. We will accommodate the needs of qualified applicants under the Human Rights Code and the Accessibility for Ontarians Disabilities Act, in all aspects of the hiring process, upon request by calling + 1 (647)724-5709 x 301. 

We thank all applicants for their interest; however, only those being considered for an interview will be contacted. In accordance with Federal Personal Information Protection and Electronic Documents Act ("PIPEDA") , personal information is collected under the authority of the Act and will only be used for candidate selection.

The base salary pay range represents the anticipated low and high range for this position. Actual salary will vary based on various factors such as the candidate’s qualifications, skills, competencies, and proficiency for the role. 

Canada Pay Range
$120$150 CAD

Skills Required

  • MS or PhD in Statistics or Biostatistics
  • PhD +4 years or MS +9 years clinical trial experience
  • Hands-on Phase I/II/III clinical trial experience
  • Proficient in SAS programming
  • Excellence in R programming desirable
  • Excellent oral and written communication skills
  • Previous experience with regulatory submissions desirable

ClinChoice Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about ClinChoice and has not been reviewed or approved by ClinChoice.

  • Flexible Benefits Flexible arrangements, including telecommuting and flextime with no core hours in some regions, are highlighted for many roles. Feedback suggests flexibility is commonly available but depends on role and location.
  • Leave & Time Off Breadth Vacation, personal, and sick days are part of the core package, with some markets granting paid leave from the date of hire. Feedback suggests time off is standard-to-decent across locations, though specifics vary.
  • Healthcare Strength Health coverage is positioned as a core benefit, with some accounts describing overall benefits as full or good. In the U.S., healthcare sits within a conventional CRO package alongside medical, dental, and vision.

ClinChoice Insights

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The Company
Horsham, Pennsylvania
5,000 Employees
Year Founded: 1995

What We Do

ClinChoice is a global full-service Contract Research Organization (CRO) specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies, aiming to accelerate the development and commercialization of innovative drugs and devices.

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