Senior Statistician — Clinical Trials Leader

Worldwide Clinical Trials; France; Sur place; EUR 60 000 - 90 000; Plein temps

Résumé du poste

Worldwide Clinical Trials is seeking a skilled Senior Statistician to join our Biostatistics and Statistical Programming team in France. You will review study designs, develop SAS programs for SDTM/ADaM datasets, and contribute to reports.

You will work with sponsors, data managers, and statisticians to ensure compliance with ICH, FDA, and other regulatory standards, while driving quality improvements across projects.

Qualifications

• Deep knowledge of SAS and CDISC standards across all phases of clinical trials.
• Experience providing statistical leadership to projects and studies.
• Excellent communication and collaboration with sponsors, data managers, and statisticians.

Responsabilités

• Provide review of study designs, analysis plans, and reports; contribute to trial design and statistical sections.
• Prepare and review tables, figures, listings, and derived datasets; format reports and tabulations.
• Develop, test, and run SAS programs for statistical analysis of clinical study data (SDTM/ADaM, tables, figures, listings).
• Identify process improvements to enhance data processing and reporting efficiency.

Connaissances

SAS

Statistical leadership

Clinical trials analysis

Regulatory knowledge

Formation

BSc/8 years

MSc/6 years

PhD/4 years

Outils

CDISC

Description du poste

Worldwide Clinical Trials is seeking a skilled Senior Statistician to join our Biostatistics and Statistical Programming team in France. You will review study designs, develop SAS programs for SDTM/ADaM datasets, and contribute to reports.

You will work with sponsors, data managers, and statisticians to ensure compliance with ICH, FDA, and other regulatory standards, while driving quality improvements across projects.