Principal Statistician

Key Information

Duration of Contract: Fixed Term for 3 years

Hours per week: 35 hours per week (Full Time) / part time working (minimum 60% FTE) will be considered. 

Location: Sutton, Surrey

This role is eligible for ICR Sponsorship. Support will be provided for costs associated with Visa application. If you are considering relocating to the UK, further information can be found here. 

We reserve the right to close this vacancy early if we receive a high volume of applications. We encourage interested candidates to apply as soon as possible to ensure consideration. Applications may be reviewed on application and not the closing of the role.

Job Details

The Cancer Research UK funded Clinical Trials and Statistics Unit at The Institute of Cancer Research (ICR-CTSU)  seek an experienced and highly motivated Principal Statistician to join their team of over 20 statisticians.

We want to hear from you if you:

• Enjoy the challenge of researching, developing and implementing efficient trial methodology, and designing efficient clinical trials that will make a difference in patients’ lives
• Seek variety in your work and opportunities to apply your statistical knowledge across multiple therapeutic areas in oncology.
• Thrive on being part of a multi-disciplinary research team with like-minded statisticians.
• Are looking to develop your career within a dynamic and supportive academic environment at a leading cancer clinical trials unit.

Key Requirements

The successful applicant will be an experienced and highly motivated medical statistician interested in researching new statistical methods and applying their statistical knowledge to the design and analysis of patient-centred clinical trials. They will have a post-graduate qualification in statistics.  They should demonstrate a solid understanding of clinical trials and experience in applying statistical methods to real-world data. Familiarity with Bayesian statistics and early phase adaptive trials are highly desirable. Effective oral and written communication skills, as well as enthusiasm for collaborating with others from diverse disciplines, are essential.   

Department/Directorate Information

ICR-CTSU manages an exciting portfolio of national and international phase II and III cancer clinical trials and an expanding number of phase I trials. You will contribute in shaping the development of methodological innovations and implementing efficient methods in new and ongoing trials, with a specific focus in early phase and adaptive trials.  You will work as part of a multi-disciplinary team on trials methodology research and on the statistical development, oversight and analysis of a number of clinical trials within the ICR-CTSU’s Early Phase and Adaptive Trials portfolio in collaboration with external organisations and the ICR/Royal Marsden Drug Development Unit.

In your supporting statement please summarise how your research/managerial experience fits with the role.  We encourage all applicants to access the job pack attached for more detailed information regarding this role.

This is an office-based role. Requests for hybrid working (splitting time between our Sutton site and home) may be considered following successful completion of key training and only if the role allows. Flexible working options may be considered.

For informal discussion about the role, please contact Professor Christina Yap, email: Christina.Yap@icr.ac.uk

For general queries about the recruitment process, please contact ICR-CTSU, email: ctsu@icr.ac.uk.