Director Biostatistics

Warman O'Brien; Remote; GBP 80,000 - 120,000; Full time

Job summary

A global pharmaceutical company in the UK is looking for a Director of Biostatistics. This role involves leading statistical strategy for oncology studies and requires extensive experience in clinical development and regulatory submissions. The ideal candidate will possess a PhD or Master's in Biostatistics and expertise in statistical strategy leadership. This is a home-based position that emphasizes cross-functional collaboration and offers the chance to contribute to advanced cancer therapies.

Qualifications

• PhD or Master’s in Biostatistics, Statistics, or related field.
• Significant oncology clinical development experience, including regulatory submissions.
• Expertise in trial design, biomarkers, and exploratory analytics.

Responsibilities

• Lead statistical strategy for haematology oncology.
• Develop integrated statistical strategies across trial phases.
• Provide cross-functional leadership for clinical and medical affairs.

Skills

Oncology clinical development experience

PhD or Master's in Biostatistics

Statistical strategy leadership

Proficiency in SAS

Experience with Bayesian methods

Leadership presence in regulatory discussions

Ability to communicate complex methods

Education

PhD or Master’s in Biostatistics or related field

Tools

SAS

R

Job description

Director Biostatistics | Global Pharma | UK | Home Based |

Global Pharma recognised for its commitment to innovation and patient impact, is expanding rapidly in the UK. As part of this growth, the company is offering a rare opportunity for a Director Biostatistics to join them.

This is an organisation where excellence is not just expected, it’s cultivated. Known for its open, forward-thinking culture and genuine commitment to purpose-driven science, the company provides an environment that inspires, supports, and rewards. Every contribution here matters. Every voice is valued. And every project pushes the boundaries of what’s possible in modern medicine.

As a Director Biostatistics you will be joining a cross-functional team that requires strong independent leadership to support clinical and observational studies, medical affairs strategies, biomarker and PK / PD analyses, or regional projects. The Director may also lead statistical efforts for early-stage assets or serve as a methodology expert, ensuring high-quality data analysis and interpretation across a variety of programs.

What you will be doing

• Lead statistical strategy for haematology oncology, serving as compound-level statistical lead across development, evidence generation, and regulatory / payer interactions.
• Develop integrated statistical strategies across trial phases (early, pivotal, RWE, post-marketing), aligned with product profile and development goals.
• Provide cross-functional leadership across clinical, medical affairs, RWE, safety, and biomarker statistics.
• Represent the organisation in global regulatory and payer discussions (FDA, EMA, PMDA, HTA), guiding statistical input for submissions and evidence packages.
• Act as an individual contributor (no line management) while mentoring study-level statisticians.
• Present findings clearly to stakeholders and leadership.
• Ensure integrated data availability for submissions and marketing support.
• Contribute to due diligence, data review, and expert statistical guidance.
• Implement and oversee advanced statistical methods.

What you will need

• PhD or Master’s in Biostatistics, Statistics, or related field.
• Significant oncology clinical development experience, including regulatory submissions and statistical strategy leadership.
• Expertise across trial design, biomarkers, exploratory analytics, RWE, safety, and post-marketing support.
• Experience with Bayesian methods, adaptive designs, external control arms, and AI / ML in clinical development.
• Knowledge of real-world data sources, integration, and interpretation.
• Recognised scientific contributions (publications, presentations, or working groups such as ASCO / ESMO).
• Strong leadership presence in external regulatory / HTA / scientific discussions.
• Proficiency in SAS (R preferred), with solid understanding of data management and programming practices.
• Experience in international teams and ability to communicate complex methods clearly.

What to do next

If this opportunity is of interest, please apply now with your CV or reach out to arrange a confidential discussion about other potential opportunities [e-mail]