Biostatistics Consultant

RPS Group Plc; Bristol; Hybrid; GBP 80,000 - 100,000; Full time

Job summary

A leading biostatistics firm is seeking Senior and Principal Biostatisticians to join their dedicated team. In this role, you will design, analyze, and interpret clinical trials, significantly influencing innovative treatments. With a focus on collaboration, you will work with diverse teams to ensure high-quality research and statistical analysis. Candidates should have extensive experience in the field, strong SAS programming skills, and possess a relevant advanced degree. Competitive salary and flexible work arrangements are offered.

Benefits

Competitive salary package

Comprehensive benefits

Bonus structure

Flexible work arrangements

Qualifications

• Minimum of 5 years as a Senior Biostatistician or 10 years for a Principal role.
• Solid understanding of advanced statistical methods and CDISC standards.
• Excellent communication skills to present complex data.

Responsibilities

• Design and implement statistical strategies for clinical trials.
• Develop statistical analysis plans and ensure their appropriateness.
• Perform statistical programming using SAS for analyses.

Skills

Statistical methods in clinical trials

SAS programming

Regulatory guidelines (FDA, EMA)

Communication skills

Problem-solving

Education

Ph.D. or Master’s in Biostatistics or Statistics

Tools

SAS

CDISC standards

Job description

Role Summary

Fortrea is looking for Senior and Principal Biostatisticians to join our sponsor‑dedicated team. As a Senior Biostatistician at Fortrea, you will play a crucial role in the design, analysis, and interpretation of clinical trials, directly impacting the development of innovative therapies and treatments. You will collaborate closely with study teams, medical experts, and project managers to ensure the highest quality scientific research and statistical analysis.

Responsibilities

• Design and implement statistical strategies for clinical trials across various therapeutic areas.
• Develop statistical analysis plans and ensure their appropriateness for study objectives.
• Perform statistical programming tasks using SAS to conduct analyses and generate study reports.
• Collaborate with cross‑functional study teams to provide statistical expertise and guidance.
• Provide expertise on statistical methodology, sample size calculations, and innovative trial design.
• Ensure the quality and integrity of statistical deliverables.
• Oversee statistical queries on multiple projects.

Experience & Qualifications

• Minimum of 5 years (Senior) or 10 years (Principal) experience as a Biostatistician within a CRO, biotech, or pharmaceutical company.
• Solid understanding of statistical methods commonly used in clinical trials, including advanced concepts.
• Extensive knowledge of CDISC standards and experience with SDTM, ADaM datasets, and TFLs.
• Proficient in base SAS, SAS macros, SAS/STAT, and debugging SAS programs.
• Strong knowledge of regulatory guidelines (e.g., FDA, EMA) and industry standards.
• Excellent communication skills with the ability to effectively collaborate and present complex data to non‑technical audiences.
• Advanced degree (Ph.D. or Master’s) in Biostatistics, Statistics, or a related field.
• Demonstrated ability to work independently, apply problem‑solving skills, and exercise sound judgment.

Benefits

We offer a competitive salary package, comprehensive benefits, and a rewarding bonus structure. Flexible work arrangements allow for a healthy work‑life balance, with the possibility of remote work from any EMEA location.

Equal Opportunity Employer

Fortrea is a proud Equal Opportunity Employer. We strive for diversity and inclusion in the workforce and do not tolerate harassment or discrimination of any kind. For more information, please visit our privacy statement and EEO policy.