Senior Statistical Programmer

Warman O'Brien; Canada; Remote; CAD 80,000 - 100,000; Full time

Job summary

An established industry player in the pharmaceutical sector is seeking a Senior Statistical Programmer to lead high-impact projects in Biometrics. This role involves tackling complex statistical programming tasks, mentoring junior team members, and ensuring data quality for clinical trials. You will collaborate directly with clients and regulatory agencies, contributing to regulatory submissions while developing innovative programming tools. Join a dynamic team that values your expertise and offers the opportunity to make a significant impact in the field of clinical research. Don’t miss this chance to advance your career in a thriving environment!

Qualifications

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

Responsibilities

• Lead statistical programming for complex projects and ensure data quality.
• Mentor junior programmers and innovate tools to enhance efficiency.

Skills

Statistical Programming

Data Quality Assurance

Regulatory Submissions

Mentoring

Clinical Trial Data Management

Education

Master’s or Ph.D. in Statistics

Master’s or Ph.D. in Biostatistics

Master’s or Ph.D. in Epidemiology

Master’s or Ph.D. in Computer Science

Tools

SAS

R

Python

Job description

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

• Mid-Senior level

Employment type

• Full-time

Job function

• Analyst, Consulting, and Research

Industries

• Pharmaceutical Manufacturing and Biotechnology Research