Principal Statistician

JR Spain; País Vasco; A distancia; EUR 60.000 - 90.000; Jornada completa

Descripción de la vacante

A leading CRO in Spain is seeking a Principal Biostatistician to lead biostatistics and programming activities for clinical studies. The role offers opportunities for career development, flexible working, and competitive benefits within a supportive company culture. Ideal candidates will have a strong background in statistical analysis and clinical trials, with proven leadership skills.

Servicios

Opportunities for career development

Flexible working platforms

Competitive benefits

Supportive company culture

Formación

• Extensive experience in clinical trials and statistical analysis.
• Proven leadership in biostatistics activities for complex programs.
• Deep knowledge of clinical trial methodology, regulations, and SAS software.

Responsabilidades

• Leading biostatistics and programming activities for studies.
• Ensuring timely, budget-compliant delivery of studies.
• Providing biostatistical input into clinical program design.

Conocimientos

Leadership

Statistical Analysis

Clinical Trial Methodology

SAS Software

Educación

M.S. or Ph.D. in statistics, biostatistics, or related field

Descripción del empleo

Social network you want to login / join with :

Senior or Principal Biostatistician – Leading CRO – Homebased – Spain

We have recently partnered with an award-winning CRO, seeking an experienced Principal Biostatistician (or Senior aiming to progress to Principal) to join their successful study delivery team. All areas of specialization are considered.

How You Will Be a Success :

As a Principal Biostatistician, you will be responsible for :

• Leading biostatistics and programming activities for a program of studies with moderate complexity and / or high impact.
• Planning, monitoring, and reviewing activities of biostatisticians and programmers.
• Ensuring timely, budget-compliant delivery of studies and analyses.
• Maintaining consistency across studies within the program.
• Providing strategic oversight, resource allocation, and team performance management.
• Leveraging regulatory experience to ensure compliance and contribute to submissions.
• Providing biostatistical input into clinical program design, including protocol development, sample size calculations, and randomization schemes.
• Contributing to CRF design, database structures, and data management coding.
• Preparing SAPs, designing analyses, and creating tables and figures for reports.
• Conducting data analysis, interpretation, and reporting.
• Supporting regulatory responses and participating in client presentations.
• Preparing research proposals and engaging in marketing presentations.

Key Qualifications and Skills :

• M.S. or Ph.D. in statistics, biostatistics, or related field.
• Extensive experience in clinical trials and statistical analysis.
• Proven leadership in biostatistics activities for complex programs.
• Excellent leadership, coaching, and mentorship abilities.
• Deep knowledge of clinical trial methodology, regulations, and SAS software.

What You Get in Return :

Opportunities for career development, flexible working platforms, competitive benefits, and a supportive company culture emphasizing work-life balance and team diversity. The organization values accountability, collaboration, partnership, and integrity, aiming to be the partner of choice in drug development.

Next Steps :

If interested, please apply with your CV promptly. For confidential discussions, contact Aimee Weston at aimeewarmanobrien.com.

J-18808-Ljbffr