Join Regeneron as a Principal Statistical Programmer specializing in SAS. Support multidisciplinary teams in clinical trial analysis and ensure data accuracy and compliance. In this role, you will provide essential programming support in line with project strategies and standards.

Collaborate effectively to lead the quality control of analysis datasets and TFLs, ensuring adherence to regulatory requirements. Your expertise will be crucial to facilitate timely and detailed reports throughout the clinical trial process. Key Responsibilities:
Support programming matters for study teams
Lead QC of analysis datasets and TFLs
Collaborate in multidisciplinary project teams
Execute project standards in programming
Ensure regulatory compliance in data reporting Requirements:
Master's Degree in relevant field
3+ years of SAS programming experience
Proficiency in SAS Base, Stat, Macro, and Graph
Solid knowledge of clinical trial analysis
Ability to adhere to project and programming standards Utilize your SAS programming skills to enhance clinical trial outcomes with Regeneron.

📌 Principal Programmer For Clinical Trials London (Canada)
🏢 Jobtailor
📍 Canada