Senior Statistical Programmer

Warman O'Brien; Fredericton; Remote; CAD 80,000 - 110,000; Full time

Job summary

A leading CRO is looking for a Senior Statistical Programmer to lead impactful projects in clinical trials. This role involves complex statistical programming tasks, client collaboration, and mentoring junior programmers. Ideal for candidates with a Master’s or Ph.D. in Statistics and significant clinical trial experience, this position offers opportunities to innovate and enhance project delivery.

Qualifications

• 6+ years of clinical trial statistical programming experience with a Master's Degree or higher.
• Experience with SDTM / ADaM datasets and regulatory submissions.

Responsibilities

• Lead statistical programming for complex projects.
• Collaborate with clients and participate in regulatory discussions.
• Mentor junior programmers and lead project teams.

Skills

Statistical Programming

Data Integrity

Mentoring

Client Collaboration

Education

Master’s or Ph.D. in Statistics

Master’s Degree or higher in a Statistical related subject

Job description

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.

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