Senior Statistician, European Clinical Trials Leader

Worldwide Clinical Trials; Austin (TX); On-site; USD 120,000 - 170,000; Full time

Job summary

Worldwide Clinical Trials in the United States seeks a Senior Statistician to independently manage statistical project support and provide expert statistical consultancy across the stats function. You will lead design reviews, analysis plans, and reporting, collaborating with sponsors and internal teams to deliver rigorous statistical solutions.

The role requires strong leadership, SAS programming, CDISC SDTM/ADaM experience, and familiarity with ICH/FDA standards.

Qualifications

• Master's level in mathematics, statistics, or another subject required with a strong statistical component.
• Minimum 3 years of statistical experience leading clinical trial projects and data analysis.
• Expert-level project statistician with leadership in projects and data analysis.

Responsibilities

• Manage statistics support for one or more projects with expert consultancy.
• Review study designs, analysis plans, and reports.
• Design of clinical trials including statistical sections and randomization methods.
• Consult with internal departments and sponsors on statistical issues and reporting requirements.
• Prepare final reports with tables, figures, listings, and data sets.
• Develop SAS programs for CDISC SDTM/ADaM datasets and validation.
• Maintain documentation of programs and validation.
• Support bidding with budget and proposals.
• Identify process improvements for data processing and reporting.

Skills

Expert project statistician

Statistical leadership

Communication & influence

Education

Master's in statistics or related

Tools

SAS

nQuery

Job description

Worldwide Clinical Trials in the United States seeks a Senior Statistician to independently manage statistical project support and provide expert statistical consultancy across the stats function. You will lead design reviews, analysis plans, and reporting, collaborating with sponsors and internal teams to deliver rigorous statistical solutions.

The role requires strong leadership, SAS programming, CDISC SDTM/ADaM experience, and familiarity with ICH/FDA standards.