Biostatistician
Remote / Online - Candidates ideally in
Southampton, Hampshire County, SO15, England, UK
Listed on 2026-09-17
Southampton, Hampshire County, SO15, England, UK
Listing for:
Kelly Science, Engineering, Technology & Telecom
Full Time, Remote/Work from Home
position Listed on 2026-09-17
Job specializations:
-
IT/Tech
Data Analyst, Data Warehousing, Information Security & Data Protection, Data Engineering
Job Description & How to Apply Below
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
- 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
- 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
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