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- Tasks: Develop and maintain Statistical Analysis Plans for oncology clinical trials.
- Company: Join a leading biotechnology firm making a real impact in cancer research.
- Benefits: Competitive salary, hybrid working, and opportunities for career progression.
- Why this job: Be part of innovative oncology studies that directly affect patient outcomes.
- Qualifications: 1-3 years experience in biostatistics or statistical programming, especially in oncology.
- Other info: Collaborative environment with a focus on professional growth and development.
The predicted salary is between 30000 - 50000 £ per year.
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
Biostatistician employer: Kelly Science, Engineering, Technology & Telecom
Contact Detail:
Kelly Science, Engineering, Technology & Telecom Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Biostatistician
✨Tip Number 1
Network like a pro! Reach out to professionals in the biostatistics field on LinkedIn or at industry events. A friendly chat can lead to opportunities that aren’t even advertised yet.
✨Tip Number 2
Show off your skills! Create a portfolio showcasing your SAS programming projects and any TFL outputs you've developed. This will give potential employers a clear view of what you can bring to the table.
✨Tip Number 3
Prepare for interviews by brushing up on your knowledge of clinical trial processes and statistical methodologies. Be ready to discuss how your experience aligns with the role, especially in oncology trials.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, we love hearing from passionate candidates like you!
We think you need these skills to ace Biostatistician
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Biostatistician role. Highlight your experience with SAS programming and any oncology trials you've worked on. We want to see how your skills match what we're looking for!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about biostatistics and how your background makes you a great fit for our team. We love seeing enthusiasm and a personal touch.
Showcase Your Collaboration Skills: Since this role involves working closely with clinical and regulatory teams, make sure to mention any relevant teamwork experiences. We value strong communication and collaboration, so let us know how you've excelled in these areas.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way to ensure your application gets into the right hands. Plus, it shows us that you’re keen on joining our team at StudySmarter!
How to prepare for a job interview at Kelly Science, Engineering, Technology & Telecom
✨Know Your Stats
Brush up on your statistical methodologies and clinical trial processes. Be ready to discuss your experience with SAP development and TFL programming, especially in oncology trials. This will show that you’re not just familiar with the concepts but can apply them practically.
✨SAS Skills on Display
Since hands-on SAS programming is crucial for this role, prepare to talk about specific projects where you used SAS for TFL development. If possible, bring examples of your work or be ready to explain your coding approach during the interview.
✨Collaboration is Key
Highlight your experience working within cross-functional teams. Be prepared to share examples of how you’ve collaborated with clinical and regulatory teams to meet project timelines and compliance standards. This shows you understand the importance of teamwork in delivering high-quality statistical deliverables.
✨Stay Updated on Regulations
Familiarise yourself with UK clinical research regulations and global trial standards. Being knowledgeable about these will not only impress your interviewers but also demonstrate your commitment to maintaining compliance in your work.