Senior Statistical Programmer 2

About the role

As a Senior Statistical Programmer 2, you will provide technical leadership across complex studies, applying advanced statistical programming expertise to ensure accurate, compliant, and submission-ready deliverables. In this role, you'll collaborate with cross-functional teams including Data Management, Biostatistics, and sponsors to drive programming strategy, oversee study deliverables, and provide guidance on data standards and regulatory requirements.

What you'll do

• Lead statistical programming activities across multiple complex clinical studies, ensuring high-quality and timely delivery of datasets, analyses, and submission packages
• Develop, validate, and review CDISC-compliant SDTM and ADaM datasets, as well as tables, figures
• Provide expert guidance on clinical database specifications, data transfer agreements, analysis datasets, TFL shells, and submission documentation
• Serve as a programming project lead, managing priorities, resources, study timelines, and stakeholder communications across internal and external teams
• Drive compliance with global regulatory requirements and industry standards, including CDISC, FDA, PMDA, ICH, GDPR, and applicable quality procedures

What you need

• 6–11 yrs of experience
• SAS
• Clinical research
• Data privacy
• SQL
• GCP
• Regulatory affairs
• Any graduate

Good to have

• VBA