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Senior Biostatistician

JR United Kingdom

Dartford

On-site

GBP 50,000 - 80,000

Full time

6 days ago
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Job summary

A leading company is looking for a highly experienced Lead Biostatistician for a long-term contract engagement. The role involves providing expert statistical leadership on clinical trial projects, supporting various aspects from study design to reporting, and collaborating with internal teams and stakeholders. Ideal candidates will have extensive experience in the pharmaceutical industry and a strong grasp of statistical methodologies and clinical trial regulations.

Qualifications

  • Extensive experience as a Lead Biostatistician in the pharmaceutical/biotech industry.
  • Strong understanding of regulatory requirements (e.g., ICH guidelines).
  • Proven ability to lead statistical aspects of clinical trials.

Responsibilities

  • Develop protocols and oversee statistical aspects of clinical trials.
  • Implement novel statistical methods and lead analyses.
  • Ensure statistical integrity of study reports.

Skills

Statistical methodologies
Clinical trial design
Excellent communication
Collaboration skills

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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