Principal Statistician

buscojobs España; Zaragoza; A distancia; EUR 50.000 - 90.000; Jornada completa

Descripción de la vacante

An established industry player is seeking a Principal Biostatistician to lead biostatistics and programming activities for impactful studies. This role offers the chance to influence clinical program design and ensure compliance with regulatory standards. The organization values diversity and collaboration, providing career progression opportunities and a supportive work environment. Join a team committed to excellence in drug development and improving patient lives. If you're ready to take your career to the next level in a flexible and rewarding setting, this opportunity is for you.

Servicios

Flexible Working Arrangements

Comprehensive Benefits Package

Career Progression Opportunities

Supportive Work Environment

Formación

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

Responsabilidades

• Leading biostatistics and programming activities for studies.
• Ensuring timely delivery of studies and analyses meeting quality standards.

Conocimientos

Statistical Analysis

Leadership

Clinical Trials

Communication Skills

Regulatory Compliance

Biostatistics

Educación

M.S. or Ph.D. in Statistics

M.S. or Ph.D. in Biostatistics

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 Statistician (or Senior aiming to progress to Principal) to join their successful study delivery team. Candidates from any area of specialization are considered.

How You Will Be a Success :

As a Principal Biostatistician, your responsibilities will include:

1. Leading biostatistics and programming activities for a program of studies with moderate complexity and/or high value and impact.
2. Planning, monitoring, organizing, and reviewing activities of biostatisticians and programmers involved in the studies.
3. Ensuring timely, budget-compliant delivery of studies and analyses meeting quality standards.
4. Maintaining consistency across studies within the program.
5. Providing strategic oversight, focusing on resource allocation and team performance.
6. Utilizing regulatory interaction experience to ensure compliance and contribute to regulatory submissions.
7. Providing biostatistical input into clinical program design, including protocol development, sample size calculations, and randomization schemes.
8. Contributing to CRF design and reviewing project database structures and data management conventions.
9. Preparing SAPs, defining derived data, and designing statistical tables and figures for reports.
10. Conducting data analysis, interpreting results, and reporting findings.
11. Writing and reviewing statistical methods sections of reports.
12. Supporting regulatory responses and participating in client and investigator presentations.
13. Preparing biostatistics input for 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 for complex programs.
• Strong leadership, coaching, and mentorship abilities.
• Knowledge of clinical trial methodology, regulatory standards, and statistical software (e.g., SAS).
• Excellent communication skills for diverse stakeholders.

What you get in return

The role offers career progression opportunities, flexible working arrangements, and a comprehensive benefits package. The company fosters a supportive environment emphasizing work-life balance and professional development.

Company culture :

The organization values diversity, accountability, collaboration, partnership, and integrity. 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 with your CV. The organization aims to onboard a new statistician promptly. For confidential discussions about other opportunities, contact Aimee Weston.