Director Biostatistics

Warman O'Brien; Remote; GBP 90,000 - 120,000; Full time

Job summary

A leading global pharma company is seeking a Director of Biostatistics to lead statistical strategies in oncological clinical development. This home-based position offers the chance to influence critical submissions and strategies across development phases. Ideal candidates will have a PhD or Master's in Biostatistics or related fields, with significant experience in regulatory submissions and statistical strategy leadership, along with strong proficiency in statistical software like SAS. If interested, please apply with your CV or reach out for a confidential discussion.

Qualifications

• PhD or Master’s in Biostatistics, Statistics, or related field required.
• Significant experience in oncology clinical development including regulatory submissions.
• Proficient with Bayesian methods, adaptive designs, and AI/ML in clinical development.

Responsibilities

• Lead statistical strategy for haematology oncology across development phases.
• Provide cross-functional leadership for clinical, medical affairs, and biomarker statistics.
• Ensure integrated data availability for submissions and marketing support.

Skills

Oncology clinical development

Statistical strategy leadership

Expertise in Bayesian methods

Proficiency in SAS

Strong leadership presence

Education

PhD or Master’s in Biostatistics, Statistics, 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]