Clinical Trials Statistics Fellow - Design & Analysis

University of Warwick

Coventry

On-site

GBP 36,000 - 47,000

Full time

9 days ago

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Benefits offered by this job

Supplement of £5,000 pro rata

Job summary

The University of Warwick invites applications for a post-graduate statistician to provide statistical input into trial design, conduct and analysis within a multi-disciplinary setting. You’ll work with the Warwick CTU to support large, multi-centre randomised trials across cancer, emergency care and other areas.

Responsibilities include independent design and analysis of trials, reporting to Data Monitoring Committees, and contributing to methodological research and systematic reviews with

Qualifications

  • PhD in Statistics/Mathematics with substantial statistics content.
  • Alternatively MSc in Medical Statistics/Statistics with substantial experience.
  • Ability to write scientific reports and manage large data sets.
  • Excellent planning and organisation skills to meet tight deadlines.
  • Strong communication skills and ability to work in a team.

Responsibilities

  • Design and analyse clinical trials in line with SOPs and GCP.
  • Prepare reports for Data Monitoring Committees and present interim results.
  • Develop trial-related projects, including secondary analyses and reviews.
  • Collaborate with CTU staff and external researchers on research questions.
  • Contribute to final reports and dissemination of findings.

Skills

Statistical analysis
Data management
Report writing
Communication
Team collaboration
Project planning

Education

PhD in Statistics/Mathematics
MSc in Medical Statistics/Statistics

Job description

The University of Warwick invites applications for a post-graduate statistician to provide statistical input into trial design, conduct and analysis within a multi-disciplinary setting. You’ll work with the Warwick CTU to support large, multi-centre randomised trials across cancer, emergency care and other areas.

Responsibilities include independent design and analysis of trials, reporting to Data Monitoring Committees, and contributing to methodological research and systematic reviews with

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