Senior Statistical Programmer - boucherville

Bilinguallink; Boucherville; Hybrid; CAD 90,000 - 130,000; Full time

Job summary

Bilinguallink is seeking a Senior/Principal Statistical Programmer to lead high-impact biometrics projects within a small CRO. The role focuses on complex statistical programming tasks, client interactions, and mentoring junior team members.

You will develop and validate SDTM/ADaM datasets, support regulatory submissions, and contribute reusable tools while ensuring data quality and project timelines in a remote/hybrid setting.

Qualifications

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

Responsibilities

• Lead statistical programming for complex projects, ensuring on-time delivery and quality.
• Provide programming oversight, project estimates, and participate in bid defenses.
• Contribute to regulatory submissions and represent the company in discussions.
• Create and validate SDTM and ADaM datasets, ensuring accuracy and data integrity.
• Mentor junior programmers and lead project teams to foster development.
• Develop macros, utilities, and tools to enhance efficiency.
• Implement data integrity checks to ensure scientific accuracy.

Skills

Statistical programming

Project leadership

Mentoring

Regulatory submissions

Data integrity

Education

Master’s or PhD in Statistics/Biostatistics/Epidemiology/CS

Tools

SAS

SDTM/ADaM

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.