Principal Statistician

JR Spain; Jaén; Presencial; EUR 60.000 - 100.000; Jornada completa

Descripción de la vacante

An established industry player is seeking a Principal Biostatistician to join their successful study delivery team. This role involves leading biostatistics and programming activities for complex clinical trials, ensuring compliance, and providing strategic oversight. The organization emphasizes career development, flexible working platforms, and a supportive culture that values accountability and collaboration. If you're passionate about making a difference in drug development and possess strong leadership skills, this opportunity is perfect for you.

Servicios

Career Development Opportunities

Flexible Working Platforms

Competitive Benefits

Supportive Company Culture

Work-Life Balance

Team Diversity

Formación

• M.S. or Ph.D. in statistics, biostatistics, or related field required.
• Extensive experience in clinical trials and statistical analysis.

Responsabilidades

• Lead biostatistics and programming activities for studies.
• Ensure timely, budget-compliant delivery of studies and analyses.

Conocimientos

Statistical Analysis

Leadership

Clinical Trials

SAS Software

Biostatistics

Educación

M.S. or Ph.D. in Statistics

Herramientas

SAS

Descripción del empleo

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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.

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