Lead Biostatistician (Remote – UK/Europe)

Worldwide Clinical Trials

Nottingham

Remote

GBP 85,000 - 110,000

Full time

13 days ago

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Job summary

Worldwide Clinical Trials is seeking a Principal Biostatistician to lead statistical strategy across multi-project portfolios. You will design, analyse, and interpret clinical data, guiding study strategies and ensuring high-quality outputs in collaboration with sponsors and cross-functional teams.

You will mentor colleagues, oversee SAS programming and SDTM/ADaM workstreams, and contribute to process improvements and regulatory readiness across diverse trials.

Qualifications

  • Lead or project biostatistician with statistical leadership across studies.
  • Strong knowledge of clinical trial design, analysis and regulatory standards.
  • Advanced SAS programming and integrity in reporting outputs.

Responsibilities

  • Lead statistical strategy, design, analysis, and reporting across projects.
  • Develop and review SAPs, protocols, randomisation, and statistical deliverables.
  • Provide expert statistical consultation to sponsors and teams.
  • Oversee SAS programs and SDTM/ADaM datasets creation and validation.
  • Deliver tables, figures, listings, and ad hoc analyses to support objectives.
  • Mentor biostatisticians in study design and methodology.
  • Contribute to quality initiatives and inspection-readiness activities.

Skills

Lead biostatistician
Statistical leadership
SAS programming
Communication skills
English proficiency

Education

BSc with 8+ years
MSc with 6+ years
PhD with 4+ years

Tools

SAS programming
SDTM/ADaM datasets

Job description

Worldwide Clinical Trials is seeking a Principal Biostatistician to lead statistical strategy across multi-project portfolios. You will design, analyse, and interpret clinical data, guiding study strategies and ensuring high-quality outputs in collaboration with sponsors and cross-functional teams.

You will mentor colleagues, oversee SAS programming and SDTM/ADaM workstreams, and contribute to process improvements and regulatory readiness across diverse trials.

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