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- Tasks: Lead programming activities for clinical trials, ensuring high-quality data delivery.
- Company: Global clinical research team with a focus on innovation and quality.
- Benefits: Remote work, competitive salary, and opportunities for professional growth.
- Why this job: Make a real impact in clinical research while working with cutting-edge technology.
- Qualifications: 5+ years of programming experience in clinical research and strong SAS skills.
- Other info: Dynamic role with mentorship opportunities and a collaborative team environment.
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.
Senior Statistical Programmer in Harlow 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 Harlow
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, attend virtual meetups, and engage on platforms like LinkedIn. We all know that sometimes it’s not just what you know, but who you know that can help you land that dream job.
✨Tip Number 2
Prepare for interviews by practising common questions and scenarios related to clinical programming. We recommend doing mock interviews with friends or using online resources to get comfortable discussing your experience with SAS and CDISC standards.
✨Tip Number 3
Showcase your skills through a portfolio! If you’ve worked on any projects or have examples of your programming work, compile them into a neat presentation. This gives potential employers a tangible sense of what you can bring to the table.
✨Tip Number 4
Don’t forget to apply through our website! We make it easy for you to find roles that match your skills and interests. Plus, it shows you’re genuinely interested in joining our team, which is always a bonus!
We think you need these skills to ace Senior Statistical Programmer in Harlow
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Senior Statistical Programmer role. Highlight your experience with SAS programming, SDTM, and ADaM datasets. 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 the perfect fit for our team. Share specific examples of your past work that relate to the responsibilities listed in the job description.
Showcase Your Problem-Solving Skills: In your application, don’t forget to mention instances where you've tackled complex problems or improved processes. We love candidates who can think strategically and bring innovative solutions to the table!
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 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 SAS macros you've created. This will show your technical expertise and how it aligns with the role.
✨Understand CDISC Standards
Familiarise yourself with SDTM and ADaM standards, as these are crucial for the position. Prepare to explain how you've applied these standards in past projects, and be ready to discuss any challenges you faced and how you overcame them.
✨Showcase Your Leadership Skills
Since this role involves leading teams, think of examples where you've successfully managed programming activities or mentored others. Highlight your ability to influence without direct authority and how you've contributed to cross-functional collaboration.
✨Prepare for Regulatory Discussions
Be prepared to talk about your understanding of global drug development regulations and submission requirements. Think of instances where you've ensured compliance in your work, as this will demonstrate your commitment to quality and attention to detail.
