Join a rapidly growing small CRO as a Principal Statistical Programmer in a remote format. Spearhead high-impact projects focused on statistical programming for clinical trials.

In this role, you will lead the programming efforts that ensure data quality and compliance with regulatory requirements. Your responsibilities will include managing timelines, mentoring junior programmers, and actively contributing to regulatory submissions. With your statistical expertise, you will innovate and develop programming tools that enhance project efficiency.

Key Responsibilities:
• Manage statistical programming for strategic clinical projects
• Guide clients through programming oversight and project defense
• Engage in regulatory submission processes and discussions
• Develop and validate SDTM and ADaM specifications
• Mentor junior programmers and foster team collaboration

Requirements:
• Master’s or Ph.D. in Statistics, Biostatistics, or related
• 6+ years' experience in clinical trial statistical programming
• Knowledge of SDTM/ADaM datasets and regulatory frameworks

Drive innovation and excel in statistical programming with this rewarding chance.
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📌 Principal Statistical Programmer - Remote (Quebec City)
🏢 Bilinguallink
📍 Quebec City