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- Tasks: Lead statistical programming for oncology studies and mentor programming teams.
- Company: Leading European CRO/consultancy with a focus on innovative clinical research.
- Benefits: Competitive hourly rate, remote work flexibility, and potential for contract extension.
- Why this job: Make a real impact in clinical research while collaborating with top professionals.
- Qualifications: Extensive SAS programming experience and strong knowledge of CDISC standards.
- Other info: Join a high-performing team dedicated to improving patient outcomes.
The predicted salary is between 36 - 60 £ per hour.
Contract Opportunity – Technical / Lead Statistical Programmer (12 Months)
Location: UK or Europe (Remote/Flexible)
Industry: CRO / Pharma
Start Date: Feb/March 2026
Contract Length: 12 Months (Strong potential for extension)
Rate: Competitive hourly rate (IR35 not applicable)
A leading European CRO/consultancy is looking for a Technical / Principal Statistical Programmer to provide programming leadership across oncology studies for a key pharmaceutical client.
Key Responsibilities- Lead statistical programming activities across multiple studies
- Develop and review SDTM and ADaM datasets in line with CDISC standards
- Produce and validate TLFs for clinical study reports and regulatory submissions
- Provide technical oversight and mentorship to programming teams
- Contribute to standards, automation, and programming efficiency initiatives
- Support development and review of SAPs and specifications
- Collaborate closely with biostatistics and data management teams
- Extensive experience in SAS programming within clinical trials
- Strong oncology experience preferred
- Expert knowledge of CDISC (SDTM / ADaM)
- Proficiency in SAS, SQL, and advanced reporting (STAT / Graph)
- Experience acting as technical lead or study lead programmer
- Background in CRO or pharmaceutical settings
- Ability to work autonomously and manage competing priorities
Join a high-performing team working on innovative clinical research with real impact for patients. This is an excellent opportunity to work on impactful development programs within a collaborative and highly respected organisation. Interested? Apply now to learn more.
Statistical Programmer in Wolverhampton employer: Warman O'Brien
Contact Detail:
Warman O'Brien Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Statistical Programmer in Wolverhampton
✨Tip Number 1
Network like a pro! Reach out to your connections in the CRO and pharma industries. Attend relevant webinars or local meetups to meet potential employers and get your name out there.
✨Tip Number 2
Show off your skills! Create a portfolio showcasing your SAS programming projects, especially those related to oncology. This will give you an edge and demonstrate your expertise to potential employers.
✨Tip Number 3
Prepare for interviews by brushing up on your technical knowledge. Be ready to discuss your experience with CDISC standards and how you've led programming activities in past roles.
✨Tip Number 4
Don’t forget to apply through our website! We’ve got loads of opportunities that might just be the perfect fit for you. Plus, it’s a great way to stay updated on new roles as they come in.
We think you need these skills to ace Statistical Programmer in Wolverhampton
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Statistical Programmer role. Highlight your experience with SAS programming, oncology studies, and CDISC standards. 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 passionate about this role and how your background makes you a perfect fit. Don’t forget to mention any relevant projects or achievements that showcase your expertise.
Showcase Your Technical Skills: Since this role involves technical leadership, be sure to highlight your proficiency in SAS, SQL, and advanced reporting. We love seeing examples of how you've used these skills in past roles, especially in CRO or pharmaceutical settings.
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 this exciting opportunity. Plus, it’s super easy!
How to prepare for a job interview at Warman O'Brien
✨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 used SAS in clinical trials, especially in oncology. Highlight any challenges you faced and how you overcame them.
✨Familiarise Yourself with CDISC Standards
Since the role requires knowledge of CDISC (SDTM/ADaM), take some time to review these standards. Be prepared to explain how you've applied them in past projects and how they impact data management and reporting.
✨Showcase Your Leadership Skills
As a Technical Lead, you'll need to demonstrate your ability to mentor and guide teams. Think of examples where you've led programming activities or contributed to team efficiency. Share how you handle competing priorities and support your colleagues.
✨Prepare for Technical Questions
Expect technical questions related to statistical programming and data analysis. Brush up on SQL and advanced reporting techniques. Practising common interview questions can help you articulate your thought process clearly during the interview.