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Senior Biostatistician

JR United Kingdom

Oxford

On-site

GBP 50,000 - 80,000

Full time

Yesterday
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Job summary

A prominent contract position for a Lead Biostatistician in Oxford, seeking an experienced professional to lend statistical expertise to clinical trials. You will support study design, oversee biostatistics deliverables, and collaborate with various stakeholders, making a significant contribution to the success of clinical projects.

Qualifications

  • Extensive experience as a Lead Biostatistician within the pharmaceutical/biotechnology industry.
  • Proven ability to lead statistical aspects of clinical trials from planning to reporting.
  • Experience of Phase II and Phase III is essential.

Responsibilities

  • Develop protocols and provide input on trial design.
  • Lead statistical analysis and reporting for multiple studies.
  • Oversee biostatistics deliverables for assigned trials.

Skills

Statistical methodologies
Clinical trial design
Regulatory requirements
Communication
Collaboration

Job description

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We are seeking a highly experienced Lead Biostatistician for a long-term contract engagement to provide expert statistical leadership on clinical trial projects.

You'll be supporting study design, protocol development, and all other statistical aspects of clinical trials.

Responsibilities:

  • Develop protocols, providing input on trial design and reporting's statistical, scientific, and operational aspects.
  • Implement novel statistical methods and innovative trial designs in collaboration with Project Statisticians.
  • Lead statistical analysis and reporting for multiple studies, including statistical deliverable meetings and exploratory analyses.
  • Oversee biostatistics deliverables for assigned trials, ensuring timely and high-quality results.
  • Collaborate with internal and external stakeholders, explaining statistical concepts to non-statisticians.
  • Ensure statistical integrity of study reports, adhering to internal standards and regulatory guidelines.
  • Support statistical programming implementation and QC.
  • Present statistical concepts to both technical and non-technical audiences.

Experience:

  • Extensive experience as a Lead Biostatistician within the pharmaceutical/biotechnology industry.
  • Strong understanding of statistical methodologies, clinical trial design, and regulatory requirements (e.g., ICH guidelines).
  • Proven ability to lead statistical aspects of clinical trials from planning to reporting.
  • Excellent communication and collaboration skills.
  • Experience of Phase II and Phase III is essential

This is a long-term contract opportunity. Please apply if interested

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