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- Tasks: Develop and maintain statistical plans for oncology trials and collaborate on impactful projects.
- Company: Join a leading biotech firm making a difference in cancer research.
- Benefits: Competitive salary, hybrid working, and opportunities for career growth.
- Why this job: Make a real impact in oncology while advancing your skills in a supportive environment.
- Qualifications: 1-3 years in biostatistics or programming, with SAS experience preferred.
- Other info: Dynamic team culture with a focus on innovation and collaboration.
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
Prepare for interviews by brushing up on your SAS programming skills and understanding the latest trends in oncology trials. We want you to shine when discussing your experience with SAPs and TFL outputs!
✨Tip Number 3
Don’t just apply; engage! When you submit your application through our website, follow up with a quick email expressing your enthusiasm for the role. It shows initiative and keeps you on their radar.
✨Tip Number 4
Showcase your collaboration skills! Be ready to discuss how you've worked with cross-functional teams in the past. Highlighting your communication prowess can set you apart from other candidates.
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 oncology trials, as these are key for us. Use specific examples that showcase your skills in SAP development and TFL programming.
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Tell us why you're passionate about biostatistics and how your background aligns with our needs. Mention any relevant projects or experiences that demonstrate your expertise in clinical trials.
Showcase Your Collaboration Skills: We love team players! In your application, emphasise your ability to work with cross-functional teams. Share examples of how you've collaborated with clinical and regulatory teams to deliver high-quality statistical outputs.
Apply Through Our Website: Don't forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows us 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, as these are crucial for the role. Show them you know your stuff!
✨SAS Skills on Display
Since hands-on SAS programming is a must-have, prepare to talk about specific projects where you've used SAS for TFL development. If possible, bring examples of your work or be ready to explain your approach to programming and validation.
✨Collaboration is Key
This role involves working closely with clinical and regulatory teams, so highlight your communication and collaboration skills. Share examples of how you've successfully worked in cross-functional teams to meet project timelines and compliance standards.
✨Regulatory Knowledge Matters
Familiarity with UK clinical research regulations is essential. Make sure you can discuss any prior involvement in regulatory submissions or CSR preparation. This will show that you understand the importance of compliance in clinical trials.