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- Tasks: You'll program TFLs for clinical reports and collaborate with teams on oncology trials.
- Company: Join a respected sponsor leading innovation in cancer research.
- Benefits: Enjoy a flexible, supportive environment with opportunities for remote work.
- Why this job: Make a real impact in oncology while working on cutting-edge clinical trials.
- Qualifications: 1-3 years of SAS programming experience in clinical trials, preferably oncology.
- Other info: Ideal for ambitious programmers eager to contribute to life-changing research.
The predicted salary is between 36000 - 60000 £ per year.
SAS Programmer – Oncology Clinical Trials (UK-based, Full Time)Join a respected sponsor driving innovation in cancer research.Are you a skilled SAS Programmer looking to contribute to life-changing oncology studies?We are partnered with an established and highly respected clinical sponsor conducting Phase II oncology trials, and we are seeking a talented SAS Programmer to support the development of TFL shells, statistical programming, and CSR deliverables.You will join a collaborative and supportive environment where your work will directly contribute to accelerating treatments for cancer patients.What You’ll Be DoingProgramming Tables, Listings, and Figures (TFLs) for clinical study reports (CSR) and interim analyses.Supporting Statistical Analysis Plan (SAP) development and updates.Collaborating with statisticians and clinical teams to deliver high-quality, regulatory-compliant outputs.Working with established SAP templates and TFL standards, using SAS as the core programming tool.Must-Have Skills & Experience1–3 years of SAS programming experience in a clinical trials setting.Experience in oncology trials (Phase I or II preferred).Hands-on experience with TFL programming and statistical outputs for CSR or interim analyses.Strong understanding of clinical trial data structures and statistical deliverables.UK-based, with the ability to collaborate with local and remote teams.Nice-to-Have SkillsFamiliarity with CDISC standards (SDTM/ADaM).Exposure to SAP development or TFL shell creation.Experience in blended or remote clinical trial teams.Knowledge of regulatory submission requirements in oncology studies.Why Join?Work with a well-respected sponsor making a meaningful impact in oncology.Gain exposure to Phase II clinical trials and regulatory-compliant deliverables.Enjoy a supportive, flexible, and collaborative environment, with a balance of independent programming and team interaction.Be part of innovative cancer research that changes patient outcomes.If you are an ambitious SAS Programmer passionate about clinical data and oncology research, we’d love to hear from you.
SAS Programmer employer: LinkedIn
Contact Detail:
LinkedIn Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land SAS Programmer
✨Tip Number 1
Network with professionals in the oncology clinical trials field. Attend industry conferences or webinars to meet potential colleagues and learn about the latest trends in SAS programming for oncology studies.
✨Tip Number 2
Familiarise yourself with CDISC standards, particularly SDTM and ADaM. Understanding these standards will not only enhance your programming skills but also demonstrate your commitment to regulatory compliance in clinical trials.
✨Tip Number 3
Engage with online communities or forums focused on SAS programming and oncology research. Sharing insights and asking questions can help you stay updated and may even lead to job referrals.
✨Tip Number 4
Consider reaching out directly to current employees at StudySmarter or similar organisations. Informational interviews can provide valuable insights into the company culture and expectations, making you a more informed candidate.
We think you need these skills to ace SAS Programmer
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your SAS programming experience, especially in clinical trials and oncology. Use specific examples of TFL programming and any relevant projects you've worked on to demonstrate your skills.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for oncology research and your understanding of the role. Mention how your experience aligns with the job requirements and express your enthusiasm for contributing to life-changing studies.
Highlight Relevant Skills: In your application, emphasise your familiarity with CDISC standards and any experience you have with SAP development or TFL shell creation. This will set you apart from other candidates.
Proofread Your Application: Before submitting, carefully proofread your application for any errors or typos. A polished application reflects your attention to detail, which is crucial in the field of clinical programming.
How to prepare for a job interview at LinkedIn
✨Showcase Your SAS Skills
Be prepared to discuss your experience with SAS programming in detail. Highlight specific projects you've worked on, especially those related to oncology trials, and be ready to explain your role in developing TFLs and statistical outputs.
✨Understand Clinical Trial Data Structures
Make sure you have a solid grasp of clinical trial data structures and the types of statistical deliverables expected in oncology studies. This knowledge will demonstrate your expertise and ability to contribute effectively to the team.
✨Familiarise Yourself with CDISC Standards
If you have experience with CDISC standards like SDTM or ADaM, be sure to mention it. Even if you don't, showing an understanding of these standards can set you apart as a candidate who is eager to learn and adapt.
✨Prepare Questions for the Interviewers
Think of insightful questions to ask about the company's approach to oncology research and the specific challenges they face. This shows your genuine interest in the role and helps you assess if it's the right fit for you.
