At a Glance
- Tasks: Analyse and report clinical trial data using advanced SAS programming skills.
- Company: Join Cytel, a leader in pharmaceutical innovation with a supportive culture.
- Benefits: Enjoy remote work flexibility, competitive salary, and continuous professional development.
- Why this job: Be part of groundbreaking patient treatment projects and make a real difference.
- Qualifications: 8+ years of SAS programming experience in clinical trials required.
- Other info: Collaborative environment with opportunities for growth and diverse perspectives.
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'll be at the heart of our client's innovation. As a Senior 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
As a Senior Statistical Programmer, you will leverage your advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADaM) to support or lead one or more Phase I-IV clinical trials. This role can be performed as fully remote.
Our values
We believe in applying scientific rigor to reveal the full promise inherent in data. We nurture intellectual curiosity and encourage everyone to approach new challenges with enthusiasm and the desire for discovery. We believe in collaboration and invite a diversity of perspectives, drawing on a variety of talents to create a wealth of possibilities. We prize innovation and seek intelligent solutions using leading-edge technology.
Responsibilities
- Performing data manipulation, analysis and reporting of clinical trial data, both safety and efficacy (ISS/ISE), utilizing SAS programming
- Generating and validating SDTM and ADaM datasets/analysis files, and tables, listings, and figures (TLFs)
- Production and QC / validation programming
- Generating complex ad-hoc reports utilizing raw data
- Applying strong understanding/experience of Efficacy analysis
- Creating and reviewing submission documents and eCRTs
- Communicating with and/or responding to internal cross-functional teams and client for project specifications, status, issues or inquiries
- Performing lead duties when called upon
- Serving as team player, with a willingness to go the extra distance to get results, meet deadlines, etc.
- Being adaptable and flexible when priorities change
Qualifications
Here at Cytel we want our employees to succeed and we enable this success through consistent training, development and support. To be successful in this position you will have:
- Bachelor’s degree in one of the following fields: Statistics, Computer Science, Mathematics, etc.
- At least 8 years of SAS programming working with clinical trial data in the Pharmaceutical & Biotech industry with a bachelor’s degree or equivalent.
- At least 6 years of related experience with a master’s degree or above.
- Study lead experience, preferably juggling multiple projects simultaneously preferred.
- Strong SAS data manipulation, analysis and reporting skills.
- Solid experience implementing the latest CDISC SDTM / ADaM standards.
- Proficiency in Efficacy analysis.
- Familiarity with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials’ data.
- Submissions experience utilizing define.xml and other submission documents.
- Experience supporting immunology, respiratory or oncology studies would be a plus.
- Excellent analytical & troubleshooting skills.
- Ability to provide quality output and deliverables, in adherence with challenging timelines.
- Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners.
Senior Statistical Programmer FSP United Kingdom and 3 (Remote) Posted on 02/26/2026 Be the Fir[...] employer: Cytel Inc
Contact Detail:
Cytel Inc Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Statistical Programmer FSP United Kingdom and 3 (Remote) Posted on 02/26/2026 Be the Fir[...]
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharmaceutical industry and let them know you're on the lookout for opportunities. A friendly chat can lead to insider info about job openings that aren't even advertised yet.
✨Tip Number 2
Prepare for interviews by practising common questions related to statistical programming and clinical trials. We recommend doing mock interviews with friends or using online platforms to get comfortable with articulating your experience and skills.
✨Tip Number 3
Showcase your expertise! Create a portfolio of your past projects, especially those involving SAS programming and CDISC standards. This will give potential employers a tangible sense of what you can bring to the table.
✨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 love seeing candidates who are proactive about their job search!
We think you need these skills to ace Senior Statistical Programmer FSP United Kingdom and 3 (Remote) Posted on 02/26/2026 Be the Fir[...]
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the skills and experiences that match the Senior Statistical Programmer role. Highlight your SAS programming expertise and any relevant experience with CDISC standards 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 specific experiences that align with the job description.
Showcase Your Team Spirit: We love team players! In your application, mention instances where you've collaborated effectively with cross-functional teams or led projects. This will show us you're ready to thrive in our dynamic environment.
Apply Through Our Website: For the best chance of success, apply directly through our website. It’s the easiest way for us to review your application and get you on board for this exciting opportunity!
How to prepare for a job interview at Cytel Inc
✨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 for data manipulation and analysis, especially in clinical trials. Highlight your experience with CDISC standards like SDTM and ADaM, as this will show you're well-prepared for the role.
✨Showcase Your Efficacy Analysis Experience
Since the role involves a strong focus on efficacy analysis, be prepared to share examples of how you've approached this in past projects. Discuss any challenges you faced and how you overcame them, as this demonstrates your problem-solving skills and analytical thinking.
✨Communicate Clearly and Confidently
Effective communication is key, especially when working with cross-functional teams. Practice explaining complex statistical concepts in simple terms. This will not only help you during the interview but also show that you can collaborate effectively with diverse teams.
✨Be Ready for Scenario-Based Questions
Expect scenario-based questions that assess your ability to handle real-world challenges in statistical programming. Think about situations where you had to adapt quickly or manage multiple projects simultaneously, and be ready to discuss how you navigated those scenarios.