Principal Statistician

buscojobs España; Barcelona; A distancia; EUR 60.000 - 100.000; Jornada completa

Descripción de la vacante

An award-winning CRO is seeking a Principal Biostatistician to lead complex study programs from a home-based location in Spain. This role involves overseeing biostatistics and programming activities, ensuring quality and compliance in clinical trials. You will be responsible for strategic oversight, resource allocation, and contributing to clinical program design. The organization offers a supportive culture that values work-life balance and career progression, making it an ideal opportunity for experienced professionals looking to make an impact in drug development.

Servicios

Flexible working environments

Career progression opportunities

Supportive culture

Work-life balance

Formación

• Extensive experience in biostatistics, especially in clinical trials.
• Proven leadership in biostatistics and programming for complex programs.

Responsabilidades

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

Conocimientos

Biostatistics

Clinical Trials

Leadership

SAS

Statistical Analysis

Communication

Educación

M.S. or Ph.D. in Statistics

Related Field

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 advance 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 value and impact.
2. Planning, monitoring, organizing, and reviewing activities of biostatisticians and programmers on the assigned 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 and resource allocation to optimize team performance.
6. Leveraging regulatory interaction experience to ensure compliance and contribute to submissions.
7. Providing biostatistical input during clinical program design, including protocol development, sample size calculations, and randomization schemes.
8. Contributing to CRF design and reviewing database structures, edit checks, and coding conventions.
9. Preparing SAPs, defining derived data, and designing tables, figures, and listings for reports.
10. Conducting data analysis, interpreting results, and reporting findings.
11. Writing and reviewing statistical methods sections of reports.
12. Supporting responses to regulatory inquiries and participating in client and investigator meetings.
13. Preparing biostatistics input for research proposals and presenting at marketing meetings.

Key Qualifications and Skills :

• M.S. or Ph.D. in statistics, biostatistics, or related field.
• Extensive experience in biostatistics, especially in clinical trials and analysis.
• Proven leadership in biostatistics and programming for complex, high-value programs.
• Strong leadership, coaching, and mentorship abilities.
• Deep knowledge of clinical trial methodology, regulations, and statistical software (e.g., SAS).
• Excellent communication skills for presenting complex data to diverse audiences.

What you get in return

Opportunities for career progression, flexible working environments, and a supportive culture that values work-life balance. The company offers competitive employment packages and a family-like atmosphere where staff are valued as individuals.

Company culture :

The organization emphasizes accountability, collaboration, partnership, and integrity, striving to deliver excellence and be the partner of choice in drug development.

What to do next :

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

For a confidential discussion about potential opportunities, please contact Aimee Weston.