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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: Flexible hours, fully remote work, and competitive remuneration package.
- 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 3-5 years of experience.
- Other info: Enjoy a healthy work-life balance and exciting career advancement opportunities.
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.
Statistical Programmer II in Basildon 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 in Basildon
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, attend relevant webinars, and join online forums. We all know that sometimes it’s not just what you know, but who you know that can help you land that Statistical Programmer II role.
✨Tip Number 2
Prepare for those interviews! Research common questions related to statistical programming and be ready to discuss your experience with SAS, CDISC, and clinical trials. We recommend practising with a friend or even in front of the mirror to boost your confidence.
✨Tip Number 3
Showcase your skills! Create a portfolio of your work, including any projects or datasets you've developed. This will give potential employers a tangible sense of your capabilities and how you can contribute to their team.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, we’re always on the lookout for talented individuals like you to join our growing organisation.
We think you need these skills to ace Statistical Programmer II in Basildon
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the skills and experiences that match the Statistical Programmer II role. Highlight your expertise in SAS, CDISC standards, and any relevant clinical trial experience to catch our eye!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about statistical programming and how your background makes you a perfect fit for our dynamic team at StudySmarter.
Showcase Your Technical Skills: Don’t forget to mention your technical skills, especially in SAS and R. We love seeing specific examples of how you've used these tools in past projects or roles, so be detailed!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the easiest way for us to receive your application and ensures you’re considered for this exciting opportunity with our growing organisation!
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.
✨Familiarise Yourself with the Company
Research the CRO's recent projects and their approach to client service. Understanding their culture and values will help you align your answers with what they’re looking for in a candidate.
✨Ask Insightful Questions
Prepare thoughtful questions about the role and the team you'll be working with. Inquire about their current projects or how they ensure high-quality deliverables, showing your genuine interest in contributing to their success.