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- 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) . Get AI-powered advice on this job and more exclusive features. Position Overview The Principal Statistical Programmer works independently with minimal supervision, tracking progress and providing expert technical support to team members. The role involves working on clinical development programs across different therapeutic areas, overseeing CRO programmers, and ensuring high-quality data summaries. Responsibilities include implementing reporting and analysis activities for clinical trials, with a focus on secondary data evaluation, HTA analyses, publications, and exploratory analyses. Responsibilities Generate analysis dataset specifications, datasets, review guides, and define.xml files for multiple studies. Develop SAS programs for datasets, listings, tables, and graphs. Deliver high-quality programming outputs, maintaining and validating SAS (and potentially R) programs. Program outputs for HTA dossiers, publications, and exploratory purposes. Understand and process data structures (CDISC or non-CDISC). Follow regulatory guidelines, including good clinical practice and electronic submissions. Contribute to standards creation, maintenance, documentation, and validation. Review and author data transfer specifications for external vendors. Collaborate with internal and external partners to meet project timelines. Review and author SOPs and work instructions related to statistical programming. Qualifications Bachelor\’s degree in computer science, data science, mathematics, or statistics. 7+ years of experience as a Statistical Programmer in a clinical development environment. Expertise in SAS programming and clinical statistical procedures. Extensive experience with CDISC standards and regulatory requirements. Experience supporting regulatory submissions and HTA dossiers is a plus. Ability to work independently with excellent communication and leadership skills. Preferred Skills Proficiency in R, Python, Java, Shiny, Markdown, Unix/Linux, git. Additional Details Location: London, England, United Kingdom Employment type: Full-time Seniority level: Mid-Senior level Job function: Information Technology Industries: Software Development #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.
