Warman O'Brien
Senior Statistical Programmer
Get notified of more jobs like this · No spam, ever
How your CV stacks up
Upload your CV to see how well it fits this job role
?%
Senior Statistical Programmer I / II | Leading CRO | Fully Remote | UK | Permanent | Excellent Salary & Benefits
An excellent opportunity for experienced Statistical Programmers to take on greater responsibility, work on exciting clinical projects, and benefit from genuine long-term career progression within a highly respected, independent CRO experiencing significant international growth.
As part of its continued European expansion, the organization is looking for several talented Senior Statistical Programmers to join its growing UK team, offering fully remote working from anywhere in the UK.
Renowned for its scientific expertise, high-quality deliverables, and strong client relationships, this organization combines the stability of an established CRO with the exciting career opportunities of a growing, ambitious business.
What really sets this opportunity apart is the investment in its people. With a strong focus on structured training, mentoring, and long-term career development, you'll have opportunities to broaden your expertise across Statistical Programming and Biostatistics, take ownership of challenging projects, and progress into future technical or leadership positions.
Reasons to use Rodeo
Start with a chat, not a search bar
Grad scheme, placement, apprenticeship? Not sure what you want yet — that's fine. Your agent talks it through with you and turns "I have no idea" into a shortlist.
It searches the market for you
Every day your agent scans the market matching roles against what actually matters to you, not just keywords on a CV.
Only hits
No noise. No "maybe this fits." Just roles with a clear explanation of why they're right — and where to focus when applying.
What you will be doing:
- Leading statistical programming activities across clinical studies.
- Developing, validating, and reviewing SDTM and ADaM datasets.
- Programming and reviewing TLFs for clinical study reports and regulatory submissions.
- Performing QC checks, resolving Pinnacle 21 issues, and preparing define.xml documentation.
- Developing SAS macros, improving programming processes, and mentoring junior programmers.
What you will need:
- Master's degree or PhD in Statistics, Biostatistics, Computer Science, or a related discipline.
- 6+ years' experience in clinical trial Statistical Programming.
- Excellent SAS programming skills; R experience advantageous.
- Strong knowledge of CDISC standards, SDTM, ADaM, and TLFs.
- Experience supporting regulatory submissions and leading programming activities.
Get help with your application
Your very own career expert that helps elevate your application to the next level.
What's in it for you:
- Fully remote working anywhere in the UK.
- Generous salary and benefits package.
- Excellent long-term career progression into technical and leadership positions.
- Strong investment in training, mentoring, and professional development.
- Opportunities to broaden your expertise across Statistical Programming and Biostatistics.
- Exposure to varied clinical studies, therapeutic areas, and international clients.
- A supportive, flexible working culture within a successful, growing CRO.
What to do next:
If this opportunity is of interest, please apply now with your CV, as interviews are being arranged as soon as possible.
Not what you're looking for? Please contact Jo Fornaciari on +44 7488 822 859 for a confidential discussion about other opportunities across Statistical Programming & Biostatistics.
“It took my CV and asked me questions relevant to understanding what kind of jobs to suggest for me. Suggestions were almost perfect. Jobs were exactly what I’ve been looking for.”
Jessica, London
Location