Regeneron is seeking a Principal Statistical Programmer. Leverage your SAS expertise to support clinical trials from programming to regulatory approval.

In this key role, your contributions will focus on guiding programming efforts aligned with project needs and standards. You'll work collaboratively with a multidisciplinary study team to ensure timely analysis and reporting in clinical trials, emphasizing data quality through regulated practices.

Key Responsibilities:
• Provide programming support to the study team
• Assist in implementing programming standards
• QC analysis datasets according to user requirements
• Engage with multidisciplinary stakeholders
• Contribute to reporting efforts until regulatory approval

Requirements:
• Master's Degree required
• 3+ years of experience in SAS programming
• Skilled in SAS Base, Stat, Macro, and Graph
• Experience with clinical trial standards
• Solid adherence to regulatory compliance

Support Regeneron's mission of quality clinical trials through your advanced SAS programming skills.
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📌 SAS Programmer for Clinical Analysis (Ontario)
🏢 Jobtailor
📍 Ontario