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- Tasks: Lead statistical programming projects and oversee CRO programmers in clinical data.
- Company: Top biostatistics firm partnering with a global pharmaceutical client.
- Benefits: Competitive salary, opportunities for impactful work, and career advancement.
- Why this job: Make a difference in patient treatment innovations and work on diverse therapeutic areas.
- Qualifications: 7+ years of experience and exceptional SAS programming skills required.
- Other info: Independent role with a chance to shape the future of healthcare.
The predicted salary is between 54000 - 84000 £ per year.
A leading biostatistics firm is searching for a Principal Statistical Programmer to work with a global pharmaceutical client in London. This senior role requires 7+ years of experience, exceptional SAS programming skills, and the ability to work independently on clinical data projects.
Responsibilities include:
- Overseeing CRO programmers
- Preparing regulatory submissions
- Ensuring high-quality deliverables
This position offers a chance to contribute to patient treatment innovations and the potential for impactful work in various therapeutic areas.
Senior Statistical Programmer - Oncology, FSP in London employer: Cytel - EMEA
Contact Detail:
Cytel - EMEA Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Statistical Programmer - Oncology, FSP in London
✨Tip Number 1
Network like a pro! Reach out to your connections in the biostatistics field, especially those who work in oncology. A friendly chat can lead to insider info about job openings or even referrals.
✨Tip Number 2
Show off your skills! Prepare a portfolio showcasing your SAS programming projects and any regulatory submissions you've worked on. This will help you stand out during interviews and demonstrate your expertise.
✨Tip Number 3
Practice makes perfect! Brush up on common interview questions for statistical programmers, especially those related to clinical data projects. We can help you with mock interviews to boost your confidence.
✨Tip Number 4
Apply through our website! We’ve got loads of opportunities that might be just what you’re looking for. Plus, applying directly can sometimes give you an edge over other candidates.
We think you need these skills to ace Senior Statistical Programmer - Oncology, FSP in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your 7+ years of experience and exceptional SAS programming skills. We want to see how your background aligns with the role, so don’t be shy about showcasing relevant projects you've worked on.
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about oncology and how your skills can contribute to patient treatment innovations. We love seeing genuine enthusiasm!
Showcase Your Independence: Since this role requires you to work independently, make sure to mention any past experiences where you successfully managed clinical data projects on your own. We want to know you can take the lead!
Apply Through Our Website: We encourage you to apply directly through our website for a smoother process. It helps us keep track of your application and ensures you don’t miss out on any important updates from us!
How to prepare for a job interview at Cytel - EMEA
✨Know Your SAS Inside Out
Make sure you brush up on your SAS programming skills before the interview. Be prepared to discuss specific projects where you've used SAS, and think about how you can demonstrate your expertise in handling clinical data. This will show them you're not just familiar with the software, but that you can leverage it effectively in real-world scenarios.
✨Showcase Your Leadership Experience
Since this role involves overseeing CRO programmers, be ready to share examples of your leadership experience. Talk about how you've managed teams or projects in the past, and highlight any challenges you faced and how you overcame them. This will help them see you as a capable leader who can guide others.
✨Prepare for Regulatory Submission Questions
Given the importance of regulatory submissions in this role, review the submission process and be prepared to discuss your experience with it. Think about specific instances where you contributed to successful submissions and what you learned from those experiences. This will demonstrate your understanding of the regulatory landscape.
✨Connect Your Work to Patient Outcomes
This position is all about contributing to patient treatment innovations, so make sure to connect your past work to real-world outcomes. Share stories about how your programming efforts have positively impacted patient care or clinical trials. This will resonate with the interviewers and show them your passion for the field.
