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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 flexible working options, competitive salary, and opportunities for 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; full-time role with a mid-senior level focus.
The predicted salary is between 48000 - 72000 £ per year.
Join to apply for the Principal Statistical Programmer FSP role at TREIZE-QUARANTE (1340).
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.
- Generating analysis dataset specifications, datasets, review guides, and defining .xml files for multiple studies.
- Developing SAS programs for datasets, listings, tables, and graphs.
- Delivering high-quality programming outputs, maintaining and validating SAS (and potentially R) programs.
- Programming outputs for HTA dossiers, publications, and exploratory purposes.
- Understanding and processing data structures (CDISC or non-CDISC).
- Following regulatory guidelines, including good clinical practice and electronic submissions.
- Contributing to standards creation, maintenance, documentation, and validation.
- Reviewing and authoring data transfer specifications for external vendors.
- Collaborating with internal and external partners to meet project timelines.
- Reviewing and authoring 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
Principal Statistical Programmer FSP employer: JobFlurry
Contact Detail:
JobFlurry Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Principal Statistical Programmer FSP
✨Tip Number 1
Network with professionals in the clinical development field, especially those who have experience as Statistical Programmers. Attend industry conferences or webinars to connect with potential colleagues and learn about the latest trends and technologies in statistical programming.
✨Tip Number 2
Familiarise yourself with the specific tools and technologies mentioned in the job description, such as SAS, R, and CDISC standards. Consider taking online courses or certifications to enhance your skills and demonstrate your commitment to staying current in the field.
✨Tip Number 3
Prepare for the interview by reviewing common questions related to statistical programming and clinical trials. Be ready to discuss your previous experiences, particularly any projects where you oversaw CRO programmers or contributed to regulatory submissions.
✨Tip Number 4
Showcase your leadership and communication skills during the application process. Highlight any experiences where you've successfully collaborated with internal and external partners, as this is crucial for the Principal Statistical Programmer role.
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 job description.
Craft a Strong Cover Letter: Write a cover letter that showcases your expertise in statistical programming and your ability to work independently. Mention specific examples of how you've contributed to clinical trials and your familiarity with regulatory guidelines.
Highlight Technical Skills: In your application, clearly list your technical skills, especially in SAS, R, and any other programming languages mentioned in the job description. Provide examples of how you've used these skills in previous roles.
Showcase Leadership Experience: If you have experience overseeing teams or collaborating with external partners, make sure to highlight this in your application. Discuss how your leadership skills have contributed to project success in past roles.
How to prepare for a job interview at JobFlurry
✨Showcase Your Technical Expertise
Make sure to highlight your experience with SAS programming and any other relevant languages like R or Python. Be prepared to discuss specific projects where you implemented statistical procedures, as this will demonstrate your capability in handling complex data.
✨Understand CDISC Standards
Since the role requires extensive knowledge of CDISC standards, brush up on these guidelines before the interview. Being able to articulate how you've applied these standards in past projects will set you apart from other candidates.
✨Demonstrate Leadership Skills
As a Principal Statistical Programmer, you'll need to lead and support team members. Prepare examples of how you've successfully managed teams or collaborated with CRO programmers to meet project timelines, showcasing your leadership abilities.
✨Prepare for Regulatory Discussions
Familiarise yourself with regulatory guidelines and good clinical practices, as these are crucial for the role. Be ready to discuss your experience with regulatory submissions and how you've ensured compliance in your previous work.
