Biostatistician

Kelly Science, Engineering, Technology & Telecom; United Kingdom; Hybrid; GBP 40,000 - 60,000; Full time

Benefits offered by this job

Competitive salary

Benefits package

Career progression

Hybrid/Remote working options

Job summary

A leading clinical research firm is seeking a Biostatistician / Statistical Programmer to join their team supporting oncology clinical trials. The role involves developing Statistical Analysis Plans, SAS programming, and ensuring statistical deliverables meet regulatory standards. The ideal candidate will have 1–3 years of relevant experience, expertise in SAS, and strong communication skills. This position offers a competitive salary and hybrid working options.

Qualifications

• 1–3 years’ experience as a Biostatistician or Statistical Programmer in oncology clinical trials.
• Hands-on experience with SAS programming for TFL development and reporting.
• Strong knowledge of clinical trial processes and statistical methodologies.

Responsibilities

• Develop and maintain Statistical Analysis Plans (SAPs) for oncology clinical trials.
• Design and program TFL shells and outputs for CSRs and interim analyses.
• Perform programming and validation using SAS in line with internal standards.

Skills

SAS programming

Statistical Analysis Plans (SAPs)

Collaboration

Communication

Understanding of oncology clinical trials

Job description

Overview

Job Title: Biostatistician / Statistical Programmer

Location: United Kingdom

Employment Type: Permanent, Full-Time

About the Role

We are seeking an experienced Biostatistician / Statistical Programmer to join our growing clinical development team, supporting Oncology Phase I–II clinical trials.

You will play a key role in SAP development and updates as well as TFL (Tables, Figures, and Listings) programming to support Clinical Study Reports (CSR) and interim analyses. This is a hands-on role working closely with clinical and regulatory teams to ensure high-quality statistical deliverables that meet regulatory and project requirements.

Responsibilities

• Develop and maintain Statistical Analysis Plans (SAPs) for oncology clinical trials
• Design and program TFL shells and TFL outputs for CSRs and interim analyses
• Collaborate with clinical and data management teams to ensure statistical deliverables meet timelines and compliance standards
• Perform programming and validation using SAS in line with internal standards
• Support data interpretation and reporting for regulatory submissions and clinical decision-making

Requirements (Must-Have)

• 1–3 years’ experience as a Biostatistician or Statistical Programmer in oncology clinical trials (Phase I/II preferred)
• Hands-on experience with SAS programming for TFL development and reporting
• Experience with SAP development and updates for clinical studies
• Strong knowledge of clinical trial processes and statistical methodologies
• Excellent communication and collaboration skills
• Experience in early-phase oncology trials
• Familiarity with UK clinical research regulations and global trial standards
• Prior involvement in regulatory submissions or CSR preparation
• Experience working within a cross-functional clinical team

What We Offer

• Competitive UK salary with benefits package
• Opportunity to work on innovative oncology studies with real patient impact
• Career progression in a growing biostatistics and clinical programming function
• Hybrid/ Remote working with a balance of home-based flexibility and in-person collaboration

Seniority level

• Mid-Senior level

Employment type

• Full-time

Job function

• Writing/Editing and Analyst

Industries

• Biotechnology Research, Pharmaceutical Manufacturing, and Medical Equipment Manufacturing

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