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- Tasks: Lead programming activities for clinical trials and ensure high-quality data delivery.
- Company: Global clinical research team focused on impactful patient outcomes.
- Benefits: Remote work, collaborative environment, and opportunities for professional growth.
- Why this job: Make a real difference in clinical research while advancing your programming skills.
- Qualifications: 5+ years of programming experience in clinical research and strong SAS proficiency.
- Other info: Join a dynamic team with minimal travel requirements and a focus on innovation.
The predicted salary is between 48000 - 72000 £ per year.
We are seeking an experienced R&D Programmer (Clinical Programming Manager) to join our global clinical research team. This role is responsible for overseeing the programming components of clinical trials — ensuring the timely, accurate, and compliant delivery of data and analyses that support regulatory submissions and scientific publications.
You’ll lead cross-functional or outsourced teams, contribute to design and analysis planning, and help standardize programming deliverables across projects to drive quality and efficiency in clinical development.
Key Responsibilities- Lead and manage programming activities across multiple clinical projects, ensuring delivery of high-quality datasets, tables, listings, and figures (T/L/G).
- Provide strong programming support for CDISC-based e-submissions, including SDTM and ADaM dataset development.
- Develop, review, and validate generic SAS macros to improve efficiency and standardization.
- Support the reporting and statistical analysis of clinical trial data, ensuring accuracy and compliance with regulatory requirements.
- Collaborate with cross-functional teams to develop programming strategies and process improvements.
- Oversee and mentor contingent workers or vendors; provide training as needed.
- Contribute to budget planning and project-level programming strategy.
- Education: Bachelor’s, Master’s, or PhD in Science, Statistics, Information Technology, or related discipline.
- Experience: Bachelor’s + 5 years or Master’s + 4 years of professional programming experience in the pharmaceutical or clinical research industry.
- Hands-on experience with SDTM, ADaM, and CDISC standards.
- Strong proficiency in SAS programming, including developing and validating clinical datasets and statistical outputs.
- Understanding of statistical models and efficacy data analysis.
- Knowledge of global drug development regulations and submission requirements.
- Strategic and analytical mindset with strong problem-solving skills.
- Excellent communication and collaboration across global and cross-functional teams.
- Ability to influence without direct authority.
- High attention to detail and commitment to quality and compliance.
- Proven ability to manage timelines and deliverables in a fast-paced environment.
This is a great opportunity to contribute to meaningful clinical research that impacts patient outcomes worldwide. You’ll work in a collaborative, innovation-driven environment with opportunities to apply advanced programming techniques and lead process improvements.
Travel Requirement: Minimal (as most tasks are performed remotely)
Contract Duration: 24 Months
Interested? Apply now or message us directly to learn more!
Senior Statistical Programmer in London employer: Radiant Systems Inc
Contact Detail:
Radiant Systems Inc Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Statistical Programmer in London
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, attend virtual meetups, and engage with professionals on LinkedIn. You never know who might have the inside scoop on job openings or can refer you directly.
✨Tip Number 2
Prepare for interviews by practising common questions and showcasing your experience with SAS programming and clinical trials. We recommend doing mock interviews with friends or using online platforms to boost your confidence.
✨Tip Number 3
Showcase your skills through a portfolio! If you’ve worked on relevant projects, compile them into a portfolio that highlights your programming expertise and contributions to clinical research. This can set you apart from other candidates.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about their job search!
We think you need these skills to ace Senior Statistical Programmer in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the skills and experiences that match the Senior Statistical Programmer role. Highlight your programming experience, especially with SAS and CDISC standards, to show us you’re the right fit!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about clinical research and how your background aligns with our mission at StudySmarter. Keep it concise but impactful!
Showcase Your Achievements: Don’t just list your responsibilities; share specific achievements in your previous roles. Whether it’s improving efficiency or leading a successful project, we want to see how you’ve made a difference!
Apply Through Our Website: We encourage you to apply directly through our website for the best chance of getting noticed. It’s quick and easy, and we can’t wait to see your application come through!
How to prepare for a job interview at Radiant Systems Inc
✨Know Your SAS Inside Out
Make sure you brush up on your SAS programming skills before the interview. Be ready to discuss specific projects where you've developed and validated clinical datasets, as well as any experience with SDTM and ADaM standards. This will show that you’re not just familiar with the tools, but that you can apply them effectively in a clinical setting.
✨Showcase Your Leadership Skills
Since this role involves leading cross-functional teams, be prepared to share examples of how you've successfully managed programming activities in previous roles. Highlight any experience mentoring others or collaborating with different departments to drive project success. This will demonstrate your ability to influence and lead without direct authority.
✨Understand Regulatory Requirements
Familiarise yourself with global drug development regulations and submission requirements. During the interview, be ready to discuss how you ensure compliance in your work. This knowledge is crucial for the role, and showing that you understand the importance of regulatory standards will set you apart from other candidates.
✨Prepare Questions About Process Improvements
Think about what process improvements you could bring to the table. Prepare thoughtful questions about the current programming strategies used by the company and how you might contribute to enhancing efficiency and quality. This shows your proactive mindset and commitment to continuous improvement, which is key in a fast-paced environment.