Principal Statistician

Warman O'Brien; Pamplona; A distancia; EUR 60.000 - 80.000; Jornada completa

Descripción de la vacante

A leading CRO in Spain is seeking an experienced Principal Biostatistician to lead biostatistics and programming activities. The role involves ensuring timely delivery of studies and providing strategic oversight. Candidates should have a strong background in clinical trials and statistical analysis, with opportunities for career progression and a flexible working environment.

Servicios

Career progression

Skill enhancement

Flexible working environment

Work-life balance

Professional development

Formación

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

Responsabilidades

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

Conocimientos

Leadership

Communication

Educación

M.S. or Ph.D. in statistics

Herramientas

SAS

Descripción del empleo

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 advance to Principal) to join their successful study delivery team. Candidates from any area of specialism 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, organizing, and reviewing activities of biostatisticians and programmers.
3. Ensuring timely, budget-compliant delivery of studies and analyses to quality standards.
4. Maintaining consistency across studies within the program.
5. Providing strategic oversight, resource allocation, and team performance management.
6. Leveraging regulatory interaction 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 structure review, and data management conventions.
• Preparing SAPs, defining derived data, and designing analysis tables and figures.
• Conducting data analysis, interpretation, and reporting.
• Writing and reviewing methods sections of reports.
• Supporting regulatory responses and participating in client meetings.
• Preparing biostatistics input for research proposals and 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 and programming for complex programs.
• Excellent leadership, coaching, and mentorship skills.
• Deep knowledge of clinical trial methodology, regulations, and SAS software.
• Strong communication skills for diverse stakeholders.

What you get in return

Opportunities for career progression, skill enhancement, and a flexible working environment. The company emphasizes work-life balance, individual respect, and professional development, offering an attractive employment package and benefits.

Company culture

The company prides itself on a diverse, collaborative culture rooted in values of accountability, partnership, integrity, and delivery. They aim to be a partner of choice in drug development, committed to excellence and improving patient lives.

What to do next

If interested, please apply now with your CV. The organization is eager to onboard a new Statistician promptly.

For confidential discussions about other opportunities, contact Aimee Weston.