Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Lead statistical programming for clinical trials and ensure high-quality data delivery.
- Company: Join a global pharmaceutical client dedicated to innovative patient treatments.
- Benefits: Enjoy autonomy, competitive salary, and opportunities for professional growth.
- Why this job: Be at the forefront of healthcare innovation and make a real difference.
- Qualifications: Extensive experience in statistical programming and strong technical skills required.
- Other info: Work in a dynamic environment with a focus on collaboration and excellence.
The predicted salary is between 36000 - 60000 £ per year.
Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you will be at the heart of our client’s innovation. This is an exciting time to be a part of this new program.
Position Overview
This position reports to the Director, Biostatistics and Programming in the FSP Services business unit in Cytel. The Principal Statistical Programmer works independently with only concept level instruction and very little supervision, tracks progress, and provides expert technical support to team members. We are looking for a highly experienced senior statistical programmer who will work on clinical development programs on different therapeutic areas and participate in overseeing CRO programmers to ensure that data summaries are delivered in a consistent, high-quality manner. This individual will be responsible for implementing all reporting and analysis activities for the Sponsor clinical trials.
As a Principal Statistical Programmer, your responsibilities will include:
- Generate SDTM, ADaM specifications, datasets, reviewer’s guide and define.xml files for multiple studies
- Develop SAS programs which generate datasets, complex listings, tables (including those with descriptive and standard inferential statistics in collaboration with a Statistician), and complex graphs
- Deliver high-quality statistical programming results including developing, validating, and maintaining SAS and/or R programs tailored to clinical development programs’ needs
- Participate in overseeing CRO’s statistical programming deliverables for multiple clinical studies to ensure high-quality and meet the pre-specified timelines
- Support the preparation of clinical study reports, regulatory submissions, publications, annual DSUR, and exploratory analyses
- Understand and follow FDA regulations which affect the reporting of clinical trial data. This includes good clinical practice and guidelines for electronic submissions.
- Contribute to the creation, maintenance, documentation, and validation of standards for programming tools, outputs, and macros
- Participate in the development of CRFs, edit check specifications, and data validation plans
- Provide review and/or author data
Principal Statistical Programmer FSP in London employer: Cytel
Contact Detail:
Cytel Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Principal Statistical Programmer FSP in London
✨Tip Number 1
Network like a pro! Reach out to professionals in the pharmaceutical industry, especially those working in statistical programming. Attend relevant events or webinars and don’t be shy about introducing yourself. You never know who might have the inside scoop on job openings!
✨Tip Number 2
Showcase your skills! Create a portfolio that highlights your best work in statistical programming. Include examples of SAS or R programs you've developed, and any impactful projects you've been part of. This will give potential employers a clear view of what you can bring to the table.
✨Tip Number 3
Prepare for interviews by brushing up on your technical knowledge and soft skills. Be ready to discuss your experience with clinical trials and how you ensure high-quality deliverables. Practise common interview questions and think of examples that demonstrate your expertise and problem-solving abilities.
✨Tip Number 4
Don’t forget to apply through our website! We’ve got loads of opportunities waiting for talented individuals like you. Make sure your application stands out by tailoring it to the specific role and showcasing your passion for innovation in patient treatment.
We think you need these skills to ace Principal Statistical Programmer FSP in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the skills and experiences that align with the Principal Statistical Programmer role. Highlight your expertise in SAS programming, clinical trials, and any relevant therapeutic areas to catch our eye!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Share your passion for statistical programming and how you can contribute to our client's innovative projects. Be sure to mention any experience overseeing CRO programmers or working independently.
Showcase Your Technical Skills: We want to see your technical prowess! Include specific examples of SAS or R programs you've developed, and any high-quality results you've delivered. This will help us understand your capabilities and how you can support our clinical development programmes.
Apply Through Our Website: Don't forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for this exciting opportunity. We can’t wait to see what you bring to the table!
How to prepare for a job interview at Cytel
✨Know Your Stuff
Make sure you brush up on your statistical programming skills, especially in SAS and R. Be ready to discuss your experience with generating SDTM and ADaM datasets, as well as any complex listings or tables you've worked on. This role requires a deep understanding of clinical trial data, so be prepared to showcase your expertise.
✨Showcase Your Autonomy
Since this position involves working independently with minimal supervision, highlight instances where you've taken ownership of projects. Share examples of how you've tracked progress and provided support to team members, demonstrating your ability to work autonomously while still being a team player.
✨Understand the Regulations
Familiarise yourself with FDA regulations and good clinical practices that impact clinical trial reporting. Being able to discuss these guidelines confidently will show that you’re not just technically skilled but also aware of the regulatory landscape, which is crucial for this role.
✨Prepare Questions
Have a few thoughtful questions ready about the company’s approach to clinical development and how they support their programmers. This shows your genuine interest in the role and helps you assess if the company culture aligns with your values, especially regarding autonomy and innovation.
