Remote Principal Statistician - Early-Phase Leader

Syneos Health Careers

United Kingdom

Remote

GBP 90,000 - 130,000

Full time

4 days ago
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Job summary

Syneos Health is seeking a Principal Statistician for Early Phase, fully home based across Europe. You will lead statistical strategy, drive trial design decisions, and mentor a team of biostatisticians.

This role supports the entire lifecycle of clinical development and requires strong collaboration with sponsors and cross-functional teams. The ideal candidate has extensive experience in clinical trials, proficiency in statistical programming, and a track record of delivering high-quality

Qualifications

  • Master's degree in biostatistics or related discipline.
  • Extensive experience in clinical trials with ability to lead multiple projects.
  • Proven ability to develop statistical strategy across development programs.
  • Strong communication skills in English; ability to collaborate with sponsors and cross-functional teams.

Responsibilities

  • Leads the development and execution of a clinical development plan and Go/No Go framework.
  • Uses simulations and statistical strategy to inform trial design decisions.
  • Mentors biostatisticians and develops training materials.
  • Directs activities of biostatistics personnel to ensure timely, high-quality work.
  • Prepares SAPs and supports data presentation for tables, listings, and figures.
  • Provides statistical programming support across the lifecycle of the project.

Skills

Biostatistics leadership
Statistical design
R programming
GCP/regulatory knowledge
Mentoring/training

Education

Master's degree in biostatistics or related discipline

Job description

Syneos Health is seeking a Principal Statistician for Early Phase, fully home based across Europe. You will lead statistical strategy, drive trial design decisions, and mentor a team of biostatisticians.

This role supports the entire lifecycle of clinical development and requires strong collaboration with sponsors and cross-functional teams. The ideal candidate has extensive experience in clinical trials, proficiency in statistical programming, and a track record of delivering high-quality

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