Lead statistical planning and delivery across clinical programs
Contribute to clinical developments plans within oncology
Work closely with clinical, regulatory, safety, data science and commercial teams
Design robust clinical trials and analyses that shape development decisions and regulatory strategy
Drive methodological innovation and mentor colleagues

Advanced degree in Statistics, Biostatistics or related quantitative discipline (MSc or equivalent)
Significant relevant post-graduate experience in oncology, within the pharmaceutical industry or a clinical research setting
Proven track record contributing statistical expertise to early and/or late phase clinical development
Practical experience implementing simulations and statistical methods using R, Python or similar tools
Clear written and verbal communication skills for explaining methods and results to non-statistical colleagues
Strong organisation and time management across multiple projects and deadlines

Associate Director – Oncology Statistics

Key skills