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Biostatistician

Stoke-on-Trent
Jr United Kingdom
Biostatistician
Posted: 24 August
Offer description

Social network you want to login/join with:

Kelly Science, Engineering, Technology & Telecom


Location:

stoke-on-trent, United Kingdom


Job Category:

Other

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EU work permit required:

Yes

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Job Views:

1


Posted:

22.08.2025


Expiry Date:

06.10.2025

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Job Description:

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.

Key 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
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