Senior Biostatistician: Clinical Trials & SAS Lead

Precision Medicine Group; Greater London; On-site; GBP 70,000 - 100,000; Full time

Job summary

Precision Medicine Group is seeking an experienced biostatistician to provide statistical support across all phases of clinical development. The role involves writing and reviewing protocols, SAPs, developing SAS programs, and presenting results to project teams and sponsors.

You will generate analysis datasets, review outputs, and serve as a biostatistical consultant to staff globally, ensuring adherence to ICH, FDA, and CDISC standards, and contributing to study budgets and regulatory

Qualifications

• Master's degree (Statistics/Biostatistics) with 10+ years experience; PhD with 7+ years.
• Experience with SAS and development of SAS programs for tables, listings, figures.
• Knowledge of ICH guidelines, CDISC data structures, 21 CFR Part 11, and FDA guidelines.
• Strong statistical concepts and techniques; oncology/rare diseases preferred.

Responsibilities

• Write and review statistical sections of protocols and SAPs.
• Develop SAS programs for tables, listings, figures, and analysis datasets.
• Lead statistical activities for studies within timelines.
• Provide input into CRFs and study design.
• Serve as biostatistical consultant to staff globally; ensure consistency across outputs.

Skills

SAS programming

Biostatistics

Statistical study design

Clinical trials

Regulatory knowledge

Project collaboration

Statistical analysis planning

Education

Master's degree in Statistics/Biostatistics

PhD in Statistics/Biostatistics

Tools

SAS

Job description

Precision Medicine Group is seeking an experienced biostatistician to provide statistical support across all phases of clinical development. The role involves writing and reviewing protocols, SAPs, developing SAS programs, and presenting results to project teams and sponsors.

You will generate analysis datasets, review outputs, and serve as a biostatistical consultant to staff globally, ensuring adherence to ICH, FDA, and CDISC standards, and contributing to study budgets and regulatory