At a Glance
- Tasks: Lead and support clinical trials using advanced SAS programming and data analysis.
- Company: Join a pioneering pharmaceutical client with a focus on innovative patient treatments.
- Benefits: Fully remote work, continuous training, and a supportive team environment.
- Other info: Collaborative culture with opportunities for professional growth and development.
- Why this job: Be at the forefront of healthcare innovation and make a real difference in patient outcomes.
- Qualifications: 8+ years of SAS programming experience in clinical trials; strong analytical skills required.
The predicted salary is between 63000 - 77000 £ per year.
Sponsor-dedicated
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 & ADa M) 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.
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 / ADa M standards.
Strong QC / validation skills.
Good ad-hoc reporting skills.
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.
How you will contribute: Performing data manipulation, analysis and reporting of clinical trial data, both safety and efficacy (ISS/ISE), utilizing SAS programming Generating and validating SDTM and ADa M 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 e CRTs 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 Full time
- Posting Date: 2026-08-05
Principal Statistical Programmer FSP in Moffat employer: Cytel
Cytel is an exceptional employer that fosters a collaborative and innovative work culture, particularly for Biostatisticians dedicated to advancing Chemistry, Manufacturing, and Control (CMC) projects. With a strong emphasis on employee development, you will benefit from consistent training and support while working closely with a global pharmaceutical client at the forefront of patient treatment. This role offers the unique opportunity to contribute to meaningful projects in a dynamic environment where your expertise in Bayesian analysis can truly make an impact.
StudySmarter Expert Advice🤫
We think this is how you could land Principal Statistical Programmer FSP in Moffat
✨Unlock Networking Opportunities
Dive into industry-specific events like pharmaceutical conferences and seminars, where you can meet hiring managers from companies like Cytel. These are goldmines for making connections and learning about job openings before they hit the mainstream job boards.
✨Join Relevant Professional Bodies
Get involved with organisations such as the Royal Pharmaceutical Society or your local pharmaceutical professionals' network. Being an active member can boost your credibility and may even lead to job referrals in top organisations like Cytel.
✨Leverage Internships for Full-time Roles
If you can, consider pursuing internships in the pharmaceutical industry, especially with companies like Cytel. These opportunities often pave the way for full-time positions and allow you to demonstrate your capabilities firsthand.
✨Tailor Your Approach
When you're applying for roles, don't rush it! Take the time to customise your applications for specific positions, showcasing relevant skills and experiences that align with what Cytel is looking for. A tailored application can really make you stand out!
We think you need these skills to ace Principal Statistical Programmer FSP in Moffat
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at Cytel!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show Cytel that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at Cytel!
Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At Cytel, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at Cytel
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Cytel that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
✨Showcase Relevant Experience
If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
✨Know Their Products
Take some time to familiarise yourself with Cytel’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.
✨Be Ready for Regulatory Scenarios
In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.
