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- Tasks: Support statistical programming for clinical trials and ensure high-quality deliverables.
- Company: Fast-growing, independent CRO with a dynamic and entrepreneurial culture.
- Benefits: Enjoy flexible hours, remote work, and a competitive salary.
- Why this job: Join a growing organisation and make a real impact in clinical research.
- Qualifications: Master’s or Ph.D. in Statistics or related field with SAS expertise.
- Other info: Great career advancement opportunities in a supportive environment.
The predicted salary is between 40000 - 50000 £ per year.
Join a fast-growing, independent CRO providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. Renowned for its high-quality deliverables, exceptional customer service, and flexibility in meeting clients’ needs, this growing organisation offers a flexible, dynamic, and entrepreneurial culture. With ongoing growth and exciting career opportunities, it’s the perfect place to advance your career.
We’re seeking several Statistical Programmers II to join this growing organisation remotely from the UK.
What you will be doing:
- You’ll support statistical programming activities across clinical trials, ensuring high-quality and timely deliverables.
- This includes developing and validating SDTM and ADaM datasets, performing QC checks, and ensuring CDISC compliance.
- You’ll assist with resolving Pinnacle 21 validation issues, contribute to the production and review of TLFs, and support regulatory submission activities.
- You will also help create define.xml files, develop and maintain SAS programs and macros, perform data integrity checks, and ensure appropriate documentation in line with SOPs.
What you will need:
- A Master’s or Ph.D. degree in Statistics, Biostatistics, Computer Science, or a related field.
- Approximately 3–5 years of experience in clinical trial statistical programming.
- Excellent knowledge of SAS is essential, with R considered advantageous.
- Good working knowledge of clinical data standards such as CDISC, SDTM, and ADaM.
- Understanding of TLFs, clinical data structures, and regulatory submission requirements.
What’s in it for you:
- The opportunity to be involved in a growing organisation.
- Enjoy a healthy work-life balance with flexible hours that fit your lifestyle.
- Fully remote role within the UK.
- Competitive remuneration package.
What to do next:
If this opportunity is of interest, please apply now with your CV, as the organisation is looking to arrange interviews for the Statistical Programmer II role as soon as possible.
Not what you’re looking for? Please contact Jo Fornaciari on +44 7488 822 859 for a confidential discussion about potential opportunities.
Statistical Programmer II employer: Warman O'Brien
Contact Detail:
Warman O'Brien Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Statistical Programmer II
✨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 related to statistical programming. Brush up on your SAS skills and be ready to discuss your experience with CDISC standards. We want you to shine when it’s your turn to impress!
✨Tip Number 3
Showcase your projects! If you've worked on relevant clinical trials or developed specific datasets, make sure to highlight these in conversations. Real-world examples 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’re always looking for talented individuals like you to join our growing team.
We think you need these skills to ace Statistical Programmer II
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience in statistical programming, especially with SAS and clinical trials. 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! Use it to explain why you’re excited about this role and how your background makes you a perfect fit. We love seeing enthusiasm and a personal touch, so let your personality come through.
Showcase Your Technical Skills: Since this role requires strong knowledge of CDISC, SDTM, and ADaM, make sure to mention any specific experiences you have with these standards. We’re looking for candidates who can hit the ground running, so highlight your technical prowess!
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’ll be able to review your application faster. Don’t miss out on this opportunity to join our dynamic team!
How to prepare for a job interview at Warman O'Brien
✨Know Your Stats
Brush up on your statistical programming knowledge, especially around SAS and CDISC standards. Be ready to discuss your experience with SDTM and ADaM datasets, as well as any challenges you've faced in previous roles.
✨Showcase Your Problem-Solving Skills
Prepare examples of how you've resolved validation issues or improved data integrity checks in past projects. This will demonstrate your ability to handle the complexities of clinical trials and regulatory submissions.
✨Understand the Company Culture
Research the organisation's values and work culture. Since they pride themselves on flexibility and customer service, think about how your personal work style aligns with these aspects and be ready to share relevant experiences.
✨Ask Insightful Questions
Prepare thoughtful questions about the role and the team you'll be working with. Inquire about their approach to maintaining high-quality deliverables and how they support professional development within the company.