Principal Statistician

hace 2 semanas


Torrejón de Ardoz, Madrid, España Warman O'Brien A tiempo completo

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. 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 program.
  3. Ensuring the timely, budget-compliant delivery of studies and analyses meeting 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.
  7. Contributing to clinical program design, including protocol input, sample size calculations, and randomization schemes.
  8. Designing statistical aspects of case report forms (CRFs).
  9. Reviewing project database structures, edit checks, and data management coding conventions.
  10. Preparing statistical analysis plans (SAP), defining derived data, and designing tables, figures, and listings.
  11. Conducting data analysis, interpreting results, and reporting findings.
  12. Writing and reviewing statistical methods sections of reports.
  13. Supporting regulatory responses and participating in client and investigator presentations.
  14. 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 biostatistics, especially in clinical trials.
  • Proven leadership in managing complex, high-value programs.
  • Excellent leadership, coaching, and mentorship abilities.
  • Deep knowledge of clinical trial methodology, regulatory standards, and statistical software (e.g., SAS).
  • Strong communication skills for presenting complex data to diverse audiences.

What you get in return

Opportunities for career progression, skill enhancement, and a supportive work environment with flexible working arrangements. The company emphasizes work-life balance and values individual staff needs, providing an attractive employment package and benefits.

Company culture :

This organization prides itself on its people. Diverse teams foster better partnerships and help fulfill their mission to improve patient lives. Their 'Own It' culture is driven by accountability, collaboration, partnership, and integrity, aiming to deliver excellence in drug development.

What to do next : If interested, please apply with your CV. The organization aims to onboard a new Statistician promptly.

Not what you're looking for? Contact Aimee Weston for a confidential discussion about other opportunities.

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