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- Tasks: Develop and maintain SAS and R programs for clinical trial data analysis.
- Company: Join a leading team in early-phase clinical programming.
- Benefits: Competitive salary, flexible work options, and opportunities for professional growth.
- Other info: Collaborative environment with a focus on innovation and quality.
- Why this job: Make a real impact on clinical trials with cutting-edge programming skills.
- Qualifications: 8+ years in Clinical SAS and 3+ years in R programming required.
The predicted salary is between 60000 - 80000 £ per year.
We are seeking an experienced Clinical SAS Programmer with strong R expertise to join our growing Early Phase SAS Programming team. In this role, you will be responsible for developing, validating, and maintaining SAS and R programs to support clinical trial reporting, data analysis, and visualization.
You will work closely with biostatisticians and cross-functional teams to deliver high-quality outputs that enhance the efficiency, quality, and success of early-phase clinical trials. This role reports to the Early Phase Programming Lead and requires the ability to work independently with minimal supervision.
Key Responsibilities- Develop, validate, and maintain SAS and R programs for clinical trial data analysis
- Design and build interactive applications using R Shiny
- Convert and optimize programs between SAS and R environments
- Generate Tables, Listings, and Figures (TFLs) for early-phase clinical studies
- Perform oversight and quality control (QC) of vendor deliverables and datasets
- Apply CDISC standards (SDTM, ADaM) in programming and data handling
- Generate and review Pinnacle 21 validation reports and data packages
- Utilize data visualization techniques (R Shiny) to support data-driven decision-making
- Ensure reproducibility by organizing code, data, and outputs into structured repositories
- Prepare and maintain technical and process documentation
- 8+ years of experience in Clinical SAS Programming
- 3+ years of hands-on experience in R programming
- Strong experience in R Shiny application development
- In-depth knowledge of CDISC standards (SDTM, ADaM)
- Experience with Pinnacle 21 validation processes
- Proven experience in generating TFLs for clinical trials
- Strong understanding of clinical trial data and regulatory requirements
- Excellent written and verbal communication skills
- Experience in early-phase (Phase I/II) clinical studies
- Exposure to data visualization and reporting automation
- Ability to work in a collaborative, fast-paced environment with minimal supervision
Clinical SAS Programmer (SAS/R) in Milton Keynes employer: princeps technologies
Contact Detail:
princeps technologies Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical SAS Programmer (SAS/R) in Milton Keynes
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical programming field, especially those who work with SAS and R. Attend industry meetups or webinars to meet potential employers and get your name out there.
✨Tip Number 2
Show off your skills! Create a portfolio showcasing your SAS and R projects, especially any interactive applications you've built using R Shiny. This will give you an edge and demonstrate your hands-on experience.
✨Tip Number 3
Prepare for interviews by brushing up on your knowledge of CDISC standards and Pinnacle 21 validation processes. Be ready to discuss how you've applied these in your previous roles, as this will show you're the right fit for the job.
✨Tip Number 4
Don't forget to apply through our website! We love seeing candidates who are genuinely interested in joining our team. Plus, it makes it easier for us to keep track of your application and get back to you quickly.
We think you need these skills to ace Clinical SAS Programmer (SAS/R) in Milton Keynes
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your 8+ years of SAS experience and 3+ years in R. We want to see how your skills match the job description, so don’t be shy about showcasing your relevant projects!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Tell us why you’re passionate about clinical trials and how your expertise in SAS and R can contribute to our Early Phase Programming team. Keep it engaging and personal!
Showcase Your Technical Skills: Don’t forget to mention your experience with CDISC standards and Pinnacle 21 validation processes. We love seeing specific examples of how you've used these in past roles, so include those details!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it’s super easy!
How to prepare for a job interview at princeps technologies
✨Know Your SAS and R Inside Out
Make sure you brush up on your SAS and R skills before the interview. Be prepared to discuss specific projects where you've developed, validated, or maintained programs. Highlight your experience with R Shiny applications and how you've used them in clinical trial data analysis.
✨Familiarise Yourself with CDISC Standards
Since the role requires knowledge of CDISC standards like SDTM and ADaM, take some time to review these concepts. Be ready to explain how you've applied these standards in your previous work, especially in generating TFLs for clinical trials.
✨Showcase Your Communication Skills
As you'll be working closely with biostatisticians and cross-functional teams, it's crucial to demonstrate your communication skills. Prepare examples of how you've effectively collaborated with others and how you ensure clarity in your technical documentation.
✨Prepare for Problem-Solving Questions
Expect questions that assess your problem-solving abilities, especially in a fast-paced environment. Think of scenarios where you've had to troubleshoot programming issues or optimise code between SAS and R. Be ready to walk through your thought process during these challenges.