Lead Statistician – Clinical Trials & SAS Expert

Worldwide Clinical Trials; United Kingdom; Presencial; GBP 48.000 - 70.000; Jornada completa

Descripción de la vacante

Worldwide Clinical Trials is seeking an experienced Biostatistician to join our UK team. You will lead statistical aspects of clinical studies, design analyses, specify listings and tables, and provide expert consultancy to sponsors and study teams.

Strong SAS programming skills and knowledge of CDISC standards are essential. You will collaborate across therapeutic areas, ensure regulatory compliance, and contribute to study design and analysis plans while mentoring junior staff in a fast-paced

Formación

• Appropriate degree and minimum relevant experience: BSc/8 years, MSc/6 years, PhD/4 years.
• Hands-on expert level project statistician experienced in providing statistical leadership to projects.
• Experience in a broad range of statistical applications across all phases of clinical research with regulatory knowledge.
• Excellent written and spoken English and ability to communicate with sponsors and study teams.

Responsabilidades

• Provide review of study designs, analysis plans, and reports; contribute to design of clinical trials and writing Statistical Analysis Plans.
• Provide support to the statistics reporting process through tables, figures, listings, and derived dataset specifications.
• Prepare final reports including production of tables, figures, listings and report writing.
• Develop, test, and run SAS programs for statistical analysis of clinical study data.
• Contribute to identifying system and process improvements to enhance efficiency and quality.

Conocimientos

SAS

Biostatistics

Statistical leadership

Client-facing consultancy

English communication

Educación

BSc in Statistics or related field

MSc in Biostatistics or related field

PhD in Biostatistics or related field

Herramientas

SAS

Descripción del empleo

Worldwide Clinical Trials is seeking an experienced Biostatistician to join our UK team. You will lead statistical aspects of clinical studies, design analyses, specify listings and tables, and provide expert consultancy to sponsors and study teams.

Strong SAS programming skills and knowledge of CDISC standards are essential. You will collaborate across therapeutic areas, ensure regulatory compliance, and contribute to study design and analysis plans while mentoring junior staff in a fast-paced