Statistics Director, Oncology
For candidates seeking to be located at our Stevenage site, this role will temporarily be based at Stevenage. However, the Company plans to relocate its offices to Cambridge, UK. The location of this role will therefore subsequently change to Cambridge, UK in accordance with timelines to be set by the Company. The relocation is currently proposed to take effect by early 2029.
At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-edge technology to transform people’s lives. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients’ needs and have the highest probability of success. We’re uniting science, technology, and talent to get ahead of disease together.
Find out more:
[Our approach to R&D](https://www.gsk.com/en-gb/innovation/)
Join GSK as a Statistics Director and take a leading role in shaping the future of how we bring new medicines to patients. You will collaborate closely with teams across research, clinical development, and external partners to apply your knowledge and drive data-driven decision making. We value curiosity, clear communication, and a passion to innovate in statistical methods that support meaningful progress in healthcare. This role offers you the chance to grow your career while making a real impact by uniting science, technology, and talent to get ahead of disease together.
Position Summary
GSK Oncology is committed to discovering and developing new therapies with the potential to change the lives of patients with cancer. The Oncology Clinical Development Statistics group is seeking exceptionally talented Statisticians to provide end-to-end statistical leadership across oncology evidence generation from early development through registration and lifecycle support using innovative trial designs and modern statistical methods (including simulation, interim strategies, Bayesian approaches, and external/real-world data) to inform key development decisions
You will lead statistical planning and delivery across clinical programs and lead clinical developments plans within oncology. You will work closely with clinical, regulatory, safety, data science and commercial teams. You will design robust clinical trials and analyses that shape development decisions and regulatory strategy. You will drive methodological innovation and mentor colleagues. Join us to grow your career, make a real impact on patient-focused R&D, and help unite science, technology and talent to get ahead of disease together.
Working model:
This role is hybrid. You will be on-site at one of the posted locations at least two days per week. Remote work is available on other days.
Responsibilities
This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:
- Represent Oncology Biostatistics externally as ap...
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