Cancer Trials Biostatistician: Design & Analyze Trials

1000scholars; Birmingham; On-site; GBP 37,000 - 46,000; Full time

Job summary

The Cancer Research UK Clinical Trials Unit (CRCTU) at the University of Birmingham seeks a Biostatistician to provide statistical expertise for the design, conduct and analysis of clinical trials. You will liaise with investigators and contribute to interim/final analyses and publications.

You will be involved in developing analysis plans, performing analyses and presenting results, while supporting compliance with GCP and related legislation.

Qualifications

• Provide statistical advice for design of clinical trials and related studies.
• Determine appropriate analysis of trial data and write statistical analysis plans.
• Undertake analysis of clinical trial data and contribute to presentations/publications.

Responsibilities

• Provide statistical advice for the design of clinical trials and related studies, and contribute to protocols and grant applications.
• Determine appropriate analysis of clinical trial data and write statistical analysis plans for trials.
• Undertake appropriate analysis of clinical trial data and prepare reports for Data Monitoring and Steering Committees and contribute to presentations and publications of clinical trial results.
• Collaborate on relevant trial-related projects with researchers in other departments within the University in terms of statistical advice and data analysis.
• Liaise with Programmers and Trial Coordinators in setting up randomisation and data collection for trials.
• Provide statistical analysis to assist Trial Coordinators in running trials and monitor data quality of ongoing trials.
• Carry out statistical methodological research relevant to cancer clinical trials and translational research with senior Biostatistics Team members.

Job description

The Cancer Research UK Clinical Trials Unit (CRCTU) at the University of Birmingham seeks a Biostatistician to provide statistical expertise for the design, conduct and analysis of clinical trials. You will liaise with investigators and contribute to interim/final analyses and publications.

You will be involved in developing analysis plans, performing analyses and presenting results, while supporting compliance with GCP and related legislation.