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- Tasks: Lead statistical programming for clinical trials and ensure high-quality data delivery.
- Company: Join a pioneering pharmaceutical client with a focus on innovative patient treatments.
- Benefits: Enjoy autonomy, competitive salary, and opportunities for professional growth.
- Other info: Collaborative environment with a focus on quality and excellence.
- Why this job: Be at the forefront of healthcare innovation and make a real difference in patient outcomes.
- Qualifications: Extensive experience in statistical programming and strong technical skills.
The predicted salary is between 60000 - 80000 £ per year.
Sponsor-dedicated: 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. As a Principal Statistical Programmer, you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next generation of patient treatment, where individuals are empowered to work with autonomy and ownership. 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.
RESPONSIBILITIES
- 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 - EMEA
Contact Detail:
Cytel - EMEA 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 and programming fields on LinkedIn. Join relevant groups, participate in discussions, and don’t hesitate to ask for informational interviews. We all know that sometimes it’s not just what you know, but who you know!
✨Tip Number 2
Prepare for those interviews by brushing up on your technical skills and understanding the latest trends in statistical programming. We recommend practising common interview questions and even doing mock interviews with friends or mentors. Confidence is key, so let’s nail that first impression!
✨Tip Number 3
Showcase your projects! If you’ve worked on any relevant programming projects or case studies, make sure to highlight them during interviews. We love seeing real-world applications of your skills, so be ready to discuss your contributions and the impact they had.
✨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 often have exclusive roles listed there, so keep an eye out for opportunities that match your expertise in statistical programming.
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 is tailored to the Principal Statistical Programmer role. Highlight your experience with SAS and R, and any relevant projects you've worked on in clinical development. We want to see how your skills align with our needs!
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 your experience with FDA regulations and high-quality programming deliverables.
Showcase Your Autonomy: Since this role requires a lot of independence, make sure to highlight instances where you've successfully worked autonomously. We love seeing examples of how you've taken ownership of projects and delivered results without much supervision.
Apply Through Our Website: We encourage you to apply through our website for the best chance of getting noticed. It’s super easy, and you’ll be able to keep track of your application status. Plus, we love seeing candidates who take that extra step!
How to prepare for a job interview at Cytel - EMEA
✨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 SDTM and ADaM specifications, as well as any complex datasets 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 technical support to team members, demonstrating your ability to lead and mentor others.
✨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 that governs the industry.
✨Prepare for Scenario Questions
Expect questions that assess your problem-solving abilities in real-world scenarios. Think about challenges you've faced in previous roles, particularly in overseeing CRO deliverables or ensuring high-quality outputs. Prepare to explain how you approached these situations and what the outcomes were.