Senior/Principal Statistical Programmer

📋 Description

• Serve as a lead statistical programmer for multiple studies and/or compounds, ensuring high-quality
• Lead and execute statistical programming activities across clinical trials, from study start-up
• Ensure consistency, quality, and executional excellence across programming deliverables for
• Support programming activities for global regulatory submissions and responses to health authority
• Provide technical oversight and guidance for outsourced statistical programming activities
• Develop, review, and validate high-quality statistical programming deliverables, including tables

🎯 Requirements

• Strong proficiency in SAS programming within a pharmaceutical, biotechnology, or CRO environment.
• Strong understanding of CDISC standards, including SDTM and ADaM.
• Hands-on experience with SDTM and ADaM specification, development, and programming.
• Strong experience in TFL programming and reporting.
• Experience supporting clinical trial reporting and/or regulatory submissions.
• Experience working with complex clinical trial data and study designs.

🎁 Benefits

• Working directly for a single sponsor while having the security and additional career opportunities
• Career opportunities within a global CRO