Senior Statistical Programmer

Warman O'Brien; Canada; Remote; CAD 110,000 - 165,000; Full time

Job summary

A leading company in biotechnology is seeking a Senior Statistical Programmer to lead high-impact projects in clinical trials. This role involves managing project timelines, ensuring data quality, and mentoring junior team members. Ideal candidates will have extensive experience in statistical programming and a strong educational background in relevant fields.

Qualifications

• 6+ years of clinical trial statistical programming experience.
• Experience with SDTM/ADaM datasets and regulatory submissions.

Responsibilities

• Lead statistical programming for complex projects.
• Collaborate with clients and ensure data quality.
• Mentor junior programmers and lead project teams.

Skills

Statistical Programming

Data Integrity

Collaboration

Education

Master’s or Ph.D. in Statistics

Job description

This range is provided by Warman O'Brien. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

CA$110,000.00/yr - CA$165,000.00/yr

Direct message the job poster from Warman O'Brien

Recruitment Team Lead | Biometrics at Warman O'Brien

Senior/Principal Statistical Programmer | Small CRO | Remote/Hybrid

We're partnered with a small CRO who are experiencing a large amount of growth within Biometrics.

The Role: As a Senior Statistical Programmer, you'll lead high-impact projects, tackling complex statistical programming tasks and managing project timelines. You'll work directly with clients and regulatory agencies, ensuring data quality and delivering programming solutions for clinical trials. You’ll also have the chance to mentor junior team members, contribute to regulatory submissions, and develop new programming tools.

Key Responsibilities:

• Lead statistical programming for complex projects, solving intricate challenges while ensuring project delivery meets quality standards.
• Collaborate with clients, providing programming oversight, project estimates, and participating in bid defenses.
• Contribute to regulatory submissions and represent the company in regulatory discussions.
• Create and validate SDTM and ADaM dataset specifications, ensuring adherence to SOPs.
• Program and validate datasets, ensuring accuracy and data integrity.
• Mentor junior programmers and lead project teams, fostering development and collaboration.
• Innovate by developing macros, utilities, and tools to enhance efficiency.
• Implement data integrity checks, ensuring scientific accuracy and quality.

Qualifications:

• Master’s or Ph.D. in Statistics, Biostatistics, Epidemiology, or Computer Science.
• 6+ years of clinical trial statistical programming experience with a Masters Degree or higher in a Statistical related subject.
• Experience working with clinical trial data, SDTM/ADaM datasets, and regulatory submissions.

What to do next?

Apply now to avoid missing out on this opportunity!

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Analyst and Science

• Industries

  Biotechnology Research and Pharmaceutical Manufacturing

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