Senior Biostatistics Lead for Phase 3 Trials

Cytel; Dover; Sur place; GBP 85 000 - 120 000; Plein temps

Résumé du poste

Cytel is seeking an Associate Director of Biostatistics to join its Global Therapeutic Statistics group in the UK. You will lead statistical activities for late-phase trials, provide development support, and collaborate with cross-functional teams to deliver regulatory-ready analyses.

We value extensive experience with SAS/R, adaptive designs, and strong communication. The role embeds with a major pharma client, offering autonomy and ownership in trial delivery.

Qualifications

• Master’s degree in Statistics or related field required.
• PhD preferred.
• 7+ years of experience supporting clinical trials in pharma/biotech.
• Strong knowledge of adaptive design, group sequential and count data methods.
• Experience in Phase II–III studies and SAP development.

Responsabilités

• Lead statistical activities for assigned Clinical Trials (Phases 3) from protocol design to reporting results.
• Represent Statistics on cross-functional trial teams and collaborate with stakeholders.
• Oversee internal programming activities and/or CRO contributions on trials.
• Contribute to or lead regulatory submissions, safety reporting, and regulatory questions.
• Collaborate with clinical, data management, programming, and other stakeholders to finalize study outputs.
• Use SAS and/or R for QC of datasets, analyses, modelling and simulations.
• Coordinate statistical activities across studies to ensure consistency and on-time delivery.

Connaissances

Statistical analysis

Cross-functional collaboration

Communication

Independent work

Project management

SAS & R proficiency

Formation

Master’s degree in Statistics or related quantitative discipline

PhD preferred

Outils

SAS

R

Description du poste

Cytel is seeking an Associate Director of Biostatistics to join its Global Therapeutic Statistics group in the UK. You will lead statistical activities for late-phase trials, provide development support, and collaborate with cross-functional teams to deliver regulatory-ready analyses.

We value extensive experience with SAS/R, adaptive designs, and strong communication. The role embeds with a major pharma client, offering autonomy and ownership in trial delivery.