Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Lead statistical programming for clinical trials, ensuring high-quality data analysis and reporting.
- Company: TREIZE-QUARANTE is a forward-thinking company focused on innovative clinical development solutions.
- Benefits: Enjoy a full-time role with opportunities for remote work and professional growth.
- Why this job: Join a dynamic team making a real impact in healthcare through data-driven insights.
- Qualifications: Bachelor's degree in relevant fields and 7+ years of experience in statistical programming required.
- Other info: Location: London; ideal for tech-savvy individuals passionate about clinical research.
The predicted salary is between 48000 - 72000 £ per year.
Join to apply for the Principal Statistical Programmer FSP role at TREIZE-QUARANTE (1340)
2 days ago Be among the first 25 applicants
Join to apply for the Principal Statistical Programmer FSP role at TREIZE-QUARANTE (1340)
Get AI-powered advice on this job and more exclusive features.
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 Principal Statistical Programmer (or, depending on your level and experience, 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.
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 Principal Statistical Programmer (or, depending on your level and experience, 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
As a Principal Statistical Programmer, you will leverage your advanced SAS programming skills and proficiency in CDISC standards (ADaM and TFL) to support programming on the basis of clinical study and project data. You will be assigned to our client\’s programming team with a responsibility for publication analyses, HTA-related data reanalysis, adhoc analyses and other challenging activities. 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.
How You Will Contribute
- Performing programming of datasets and outputs based on customer internal requests, using predominantly SAS, in an environment that requires flexibility and independence.
- Generating and validating ADaM datasets/analysis files, and tables, listings, and figures (TLFs) for clinical studies in phase 1-4 and potentially for pooled analyses (like ISS/ISE)
- Production and QC / validation programming
- Generating complex ad-hoc reports utilizing raw data
- Applying strong understanding/experience of Efficacy analysis
- Creating and reviewing related documents
- 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
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
- Bachelors degree in one of the following fields Statistics, Computer Science, Mathematics, etc.
- At least 6 years of SAS programming working with clinical trial data in the Pharmaceutical & Biotech industry with a bachelors degree or equivalent. At least 4 years of related experience with a masters degree or above. Knowledge of early phase/PK/PD could be a plus.
- Strong SAS data manipulation, analysis and reporting skill. R knowledge is a plus.
- Solid experience implementing the latest CDISC ADaM 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.
- Experience supporting neuroscience or immunotherapy projects would be a plus.
- Excellent analytical & troubleshooting skills.
- Ability to provide quality output and deliverables, in adherence with challenging timelines.
- Flexible, independent mindset; self-organized and a good communicator and team player.
- Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners.
Cytel Inc. is an Equal Employment / Affirmative Action Employer. Applicants are considered for all positions without regard to race, color, religion, sex, national origin, age, veteran status, disability, sexual orientation, gender identity or expression, or any other characteristics protected by law.
LNKD1_UKTJ
Seniority level
-
Seniority level
Mid-Senior level
Employment type
-
Employment type
Full-time
Job function
-
Job function
Information Technology
-
Industries
Software Development
Referrals increase your chances of interviewing at TREIZE-QUARANTE (1340) by 2x
Junior Data Scientist – Quantitative Market Research (Agency Side)
London, England, United Kingdom 3 weeks ago
London, England, United Kingdom 10 months ago
London, England, United Kingdom 21 hours ago
London, England, United Kingdom 7 months ago
London, England, United Kingdom 19 hours ago
London, England, United Kingdom 10 months ago
Statistical Analyst (London, Entry Level)
London, England, United Kingdom 3 days ago
London, England, United Kingdom 1 month ago
London, England, United Kingdom 9 hours ago
City Of London, England, United Kingdom £80,000.00-£90,000.00 1 day ago
London, England, United Kingdom 1 week ago
Quantitative Researcher – Systematic Equities
London, England, United Kingdom 6 days ago
London, England, United Kingdom 5 days ago
Quantitative Researcher, Systematic Equities
Greater London, England, United Kingdom 1 week ago
City Of London, England, United Kingdom £80,000.00-£80,000.00 1 week ago
London, England, United Kingdom 8 hours ago
London, England, United Kingdom 1 month ago
Quantitative Researcher – Fundamental Equities
City Of London, England, United Kingdom £80,000.00-£80,000.00 2 weeks ago
London, England, United Kingdom 1 month ago
London, England, United Kingdom 2 weeks ago
London Area, United Kingdom £45,000.00-£55,000.00 1 month ago
London, England, United Kingdom 1 week ago
We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-Ljbffr
Principal Statistical Programmer FSP employer: TREIZE-QUARANTE (1340)
Contact Detail:
TREIZE-QUARANTE (1340) Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Principal Statistical Programmer FSP
✨Tip Number 1
Familiarise yourself with the latest CDISC standards and regulatory guidelines. This knowledge will not only help you in interviews but also demonstrate your commitment to maintaining high-quality data summaries, which is crucial for the role.
✨Tip Number 2
Network with professionals in the clinical development field, especially those who work with CROs. Engaging with others can provide insights into the role and may even lead to referrals, increasing your chances of landing the job.
✨Tip Number 3
Brush up on your SAS programming skills and consider showcasing any relevant projects or contributions you've made in the past. Being able to discuss your programming outputs confidently can set you apart from other candidates.
✨Tip Number 4
Prepare to discuss your experience with HTA analyses and regulatory submissions during the interview. Highlighting your expertise in these areas will show that you understand the complexities of the role and are ready to contribute from day one.
We think you need these skills to ace Principal Statistical Programmer FSP
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in statistical programming, particularly with SAS and CDISC standards. Emphasise your 7+ years of experience in clinical development and any specific projects that align with the responsibilities listed in the job description.
Craft a Strong Cover Letter: In your cover letter, express your enthusiasm for the role and the company. Discuss how your skills and experiences make you a perfect fit for the Principal Statistical Programmer position, focusing on your ability to work independently and lead projects.
Showcase Technical Skills: Clearly outline your technical skills in SAS programming, R, and any other relevant programming languages. Provide examples of how you've used these skills in past roles, especially in relation to regulatory submissions and HTA dossiers.
Highlight Collaboration Experience: Since the role involves collaboration with internal and external partners, include examples of successful teamwork in your application. Mention any leadership roles or instances where you contributed to project timelines and standards creation.
How to prepare for a job interview at TREIZE-QUARANTE (1340)
✨Showcase Your Technical Expertise
Be prepared to discuss your experience with SAS programming and any other relevant languages like R or Python. Highlight specific projects where you implemented complex statistical procedures, as this will demonstrate your capability to handle the technical demands of the role.
✨Understand Regulatory Guidelines
Familiarise yourself with good clinical practice and regulatory requirements, especially those related to CDISC standards. Being able to articulate your understanding of these guidelines will show that you are well-prepared for the responsibilities of the position.
✨Demonstrate Leadership Skills
Since the role involves overseeing CRO programmers and collaborating with various partners, be ready to share examples of how you've successfully led teams or projects in the past. This will highlight your ability to work independently while also guiding others.
✨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving skills in real-world scenarios. Think about challenges you've faced in previous roles, particularly in clinical trials, and how you overcame them. This will help illustrate your analytical thinking and adaptability.
