Associate Director Biostatistics
Listed on 2026-10-30
-
Science
Clinical Research
Associate Director, Biostatistics (Asset Lead)
Impact: Lead statistical strategy and decision‑making across registration‑directed clinical programmes
About the OrganisationJoin a large, well‑capitalised global pharmaceutical organisation with a strong and growing US presence. The company is making sustained investments across its clinical development portfolio, with a clear focus on modernising trial design, strengthening evidence generation, and elevating quantitative science as a core driver of success.
Biostatistics is positioned as a strategic scientific function, with statisticians embedded directly into development decision‑making rather than operating as a downstream service.
Why This Role ExistsAs the clinical pipeline expands, the organisation is strengthening its statistical leadership bench. This hire is designed to bring in a senior‑level statistician who can operate with autonomy, take ownership of complex studies, and partner credibly with senior Clinical, Regulatory, and Medical stakeholders.
This is a key role within the biometrics group, offering high visibility and genuine influence across active clinical programmes.
What You’ll Do- Act as asset‑level statistical lead, owning studies from design through analysis and submission
- Define and execute statistical strategy for registration‑directed trials
- Author and oversee SAPs, analysis plans, and reporting deliverables
- Provide input into study design, endpoints, and analysis approach
- Guide simulation work and innovative design considerations where appropriate
- Partner closely with Clinical Development, Regulatory, Medical, and Data Science teams
- Represent Biostatistics in cross‑functional governance and decision forums
- Ensure high‑quality, timely delivery through internal teams and external vendors
- PhD in Biostatistics, Statistics, or a related discipline
- ~8–10+ years of industry experience in clinical development
- Experience leading Phase I–IV clinical trials
- Strong understanding of statistical methodology and its clinical application
- Confidence handling missing data strategies and regulatory‑grade analyses
- Ability to communicate complex statistical concepts to non‑statisticians
- Experience with SAS; R exposure for simulation work is beneficial
- True asset ownership and accountability
- Statisticians positioned as decision‑makers, not support resources
- High visibility within a growing US development organisation
- Opportunity to influence study design and evidence strategy
- Competitive compensation and long‑term growth potential
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).