Senior Statistician - Lead Analytics for Global Trials

Worldwide Clinical Trials; Madrid; Presencial; EUR 55.000 - 75.000; Jornada completa

Descripción de la vacante

Worldwide Clinical Trials is seeking a senior statistician to join our Biostatistics team in Madrid. You will contribute to study design, analysis plans, and reporting, while developing SAS programs for a range of clinical study data.

The role requires deep experience in clinical research, strong English communication, and the ability to oversee multiple projects with independence and rigor.

Formación

• Appropriate degree and minimum relevant experience: (BSc/8 years, MSc/6 years, PhD/4 years)
• Hands-on expert level project statistician with leadership experience on projects.
• Broad range of statistical applications across all phases of clinical research with regulatory exposure.
• Excellent oral and written communication in English.
• Ability to prioritize and manage multiple projects simultaneously with independent judgement.
• Experience across multiple therapeutic areas.

Responsabilidades

• Provide statistical leadership and review study designs, analysis plans, and reports.
• Develop, test, and run SAS programs for statistical analyses of clinical study data.
• Prepare final reports including tables, figures, and listings; contribute to study reports and documentation.
• Ensure compliance with regulatory standards (ICH, FDA) and sponsor quality systems.
• Identify process improvements to enhance efficiency and quality of data processing and reporting.
• Liaise with sponsors, data managers, statisticians, and study teams across therapeutic areas.

Conocimientos

SAS

Statistics

Clinical trial experience

English communication

Educación

BSc/8 years

MSc/6 years

PhD/4 years

Herramientas

SAS

Descripción del empleo

Worldwide Clinical Trials is seeking a senior statistician to join our Biostatistics team in Madrid. You will contribute to study design, analysis plans, and reporting, while developing SAS programs for a range of clinical study data.

The role requires deep experience in clinical research, strong English communication, and the ability to oversee multiple projects with independence and rigor.