Job Search and Career Advice Platform

Enable job alerts via email!

Senior Statistician

The Institute of Cancer Research

Sutton

Hybrid

GBP 125,000 - 150,000

Full time

Today
Be an early applicant

Generate a tailored resume in minutes

Land an interview and earn more. Learn more

Job summary

A leading cancer research institute in Sutton, UK is seeking an experienced Senior or Principal Statistician to enhance clinical trial methodologies. Candidates should possess a postgraduate qualification in statistics, strong skills in statistical analysis, and a passion for applying their knowledge in real-world scenarios. The role offers full-time hours, with hybrid work options after training, and involves participating in innovative cancer clinical trials. Join a diverse and inclusive team dedicated to impactful research.

Benefits

Exclusive staff benefits
Support for visa application
Inclusive work environment

Qualifications

  • Experience in designing and analyzing clinical trials.
  • Solid understanding of statistical methods and their application.
  • Familiarity with early phase adaptive trials is desirable.

Responsibilities

  • Research and develop trial methodologies.
  • Design clinical trials that improve patient outcomes.
  • Collaborate on statistical development and analysis.

Skills

Research methodology
Statistical analysis
Bayesian statistics
Communication skills
Team collaboration

Education

Postgraduate qualification in statistics
Job description
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

Closing Date: 11th February 2026

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

The Cancer Research UK funded Clinical Trials and Statistics Unit at The Institute of Cancer Research (ICR-CTSU) seek an experienced and highly motivated statistician to join our team of over 20 statisticians and methodologists. This position will be appointed at either Senior Statistician or Principal Statistician level, depending on the successful candidate’s experience and qualification.

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 as part of a multi‑disciplinary research team alongside like‑minded statisticians and methodologists
  • 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 hold a postgraduate qualification in statistics and demonstrate a solid understanding of clinical trials, with experience in applying statistical methods to real‑world data. Familiarity with Bayesian statistics and early phase adaptive trials is highly desirable. Strong oral and written communication skills, and enthusiasm for collaborating across diverse disciplines, are essential.

Department/Directorate Information

ICR-CTSU manages an exciting portfolio of national and international cancer clinical trials across all phases. You will contribute to methodological innovations and implement efficient methods in new and ongoing trials, with a particular 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 several 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 indicate whether you are applying for the Senior or Principal Statistician role and summarise how your experience aligns with the requirements.

We encourage all applicants to access the attached job pack 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: [emailprotected]

For general queries about the recruitment process, please contact ICR-CTSU, email: [emailprotected].

About The Institute of Cancer Research

Why work for us?

As a member of staff, you’ll have exclusive access to a range of staff benefits.

The ICR is committed to supporting overseas applicants applying for roles, please click here to find out further information.

The Institute of Cancer Research, London, is one of the world’s most influential cancer research institutes, with an outstanding record of achievement dating back more than 100 years. Further information about working at the ICR can be found here.

At the Institute of Cancer Research, we champion diversity as we believe it fuels innovation and drives impactful research. We welcome applicants from all walks of life, valuing diverse perspectives that enrich our work.

Don’t let a checklist of qualifications hold you back – if you’re passionate about the role, we want to hear from you. Your unique experiences and backgrounds contribute to the richness of our team. We are committed to being an equal opportunity for all, regardless of ethnicity, gender, age, sexual orientation, disability, or any other dimension of diversity. Join us in creating an inclusive environment where everyone’s voice is heard and valued.

Get your free, confidential resume review.
or drag and drop a PDF, DOC, DOCX, ODT, or PAGES file up to 5MB.