• 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

#J-18808-Ljbffr

📌 Principal Statistical Programmer (Markstay-Warren)
🏢 Jobtailor
📍 Markstay-Warren