Principal Statistician

JR Spain; España; A distancia; EUR 50.000 - 90.000; Jornada completa

Descripción de la vacante

An award-winning CRO is seeking a Principal Biostatistician to lead biostatistics and programming for impactful studies. This role offers the chance to work on diverse projects, ensuring compliance and strategic oversight while mentoring a talented team. With a focus on career development and work-life balance, this innovative firm values collaboration and integrity, making it an ideal environment for professionals eager to advance in drug development. Join a supportive culture that emphasizes accountability and diversity, and take your career to the next level!

Servicios

Flexible working platforms

Career development opportunities

Competitive benefits

Supportive company culture

Work-life balance

Formación

• Extensive experience in clinical trials and statistical analysis.
• Proven leadership in biostatistics activities for complex programs.

Responsabilidades

• Leading biostatistics and programming activities for a program of studies.
• Ensuring timely, budget-compliant delivery of studies and analyses.

Conocimientos

Biostatistics

Statistical Analysis

Leadership

Clinical Trials

SAS Software

Communication Skills

Educación

M.S. or Ph.D. in Statistics

Relevant Field

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:

1. Leading biostatistics and programming activities for a program of studies with moderate complexity and/or high impact.
2. Planning, monitoring, and reviewing activities of biostatisticians and programmers.
3. Ensuring timely, budget-compliant delivery of studies and analyses.
4. Maintaining consistency across studies within the program.
5. Providing strategic oversight, resource allocation, and team performance management.
6. Leveraging regulatory experience to ensure compliance and contribute to submissions.

Desirable Experience:

• 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.
• Strong communication skills for diverse stakeholders.

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.