• Provide timely support to the study team on all programming matters according to the project strategies
• Assist in providing guidance in implementing and executing the programming and project standards
• Support and/or lead programmer for programming and QC of analysis datasets, TFLs or standard tools following Regeneron standard data models or user requirements
• Work in a multidisciplinary study team to provide timely and quality support for analysis and reporting of clinical trials up to regulatory approval
Requirements
Masters Degree
SAS (Base, Stat, Macro, graph)
3+ Years experience
Core Competencies
Demonstrates expertise in SAS programming, including Base, Stat, Macro, and Graph, to support clinical trial analysis and reporting.



Collaborates effectively within multidisciplinary teams to ensure adherence to project standards and regulatory requirements.
Highest-signal resume keywords
SAS Programming
Clinical Trial Analysis
Data Quality Control
Regulatory Compliance
Masters Degree
ATS Optimization Keywords
Hard Skills
SAS Base
SAS Stat
SAS Macro
SAS Graph
Programming Standards
Data Analysis
Data Reporting
QC of Analysis Datasets
TFLs
User Requirements
Industry Keywords
Clinical Trials
Regulatory Approval
Multidisciplinary Team
Project Strategies
Data Models

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📌 Principal Statistical Programmer (Ontario)
🏢 Jobtailor
📍 Ontario