Principal Statistical Programmer (R Programming)
Principal Statistical Programmer (R Programming)

Principal Statistical Programmer (R Programming)

Looe Full-Time 36000 - 60000 £ / year (est.) No home office possible
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IQVIA

At a Glance

  • Tasks: Lead R programming for clinical trials and develop innovative statistical solutions.
  • Company: Join IQVIA, a global leader in clinical research and healthcare intelligence.
  • Benefits: Competitive salary, flexible work options, and opportunities for professional growth.
  • Why this job: Make a real impact on patient outcomes through advanced statistical programming.
  • Qualifications: 5+ years of R programming experience in clinical trials and strong data analysis skills.
  • Other info: Collaborative team environment with a focus on innovation and career advancement.

The predicted salary is between 36000 - 60000 £ per year.

Join a sponsor-dedicated team and contribute to the advancement of in-house study activities over time. As the R Programming Lead, you will provide technical expertise to the Statistical Programming team, ensuring the delivery of high-quality solutions that meet both internal and external requirements.

Responsibilities

  • Develop internal and external R packages for clinical trial analysis (ADaM, tables, figures, listings).
  • Validate R packages.
  • Lead implementation in R and train other Biostatistics team members.
  • Conduct statistical programming work of clinical data using R.
  • Identify problems and develop global tools that increase the efficiency and capacity of the Statistical Programming group.
  • Create and/or validate all safety and efficacy study output requirements (e.g. ADaM, TLFs) consistent with data definitions and specifications and relevant study documentation (e.g. protocol, SAP, aCRF).
  • Collaborate with peers and statisticians to ensure the quality and accuracy — thus submission readiness — of clinical data as required by authorities (e.g. SDTM, ADaM, tables, figures, listings, define.xml).

Experience and Qualifications

  • Minimum 5+ years of experience in R programming for clinical trial data including developing and validating R packages from CRO or Pharmaceutical Industry.
  • Strong programming skills in R/R Shiny
  • Proven experience in applying R and R-Shiny for the analysis and reporting of clinical trials. Ability to reproduce statistical analysis using R.
  • Strong skills in data visualization and data wrangling using R. Proficiency in using R packages for data exploration and visualization.
  • Application of statistical methodology and concepts in clinical trial analysis. Experience with R-Shiny apps for data exploration.
  • Advanced knowledge of industry standards including CDISC data structures as well as a solid understanding of the development and use of standard programs.
  • In-depth understanding of the phases of clinical trials and the drug development process.
  • Exposure to Late Phase & Real-World Evidence (RWE) studies is highly desirable.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

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Principal Statistical Programmer (R Programming) employer: IQVIA

At IQVIA, we pride ourselves on being an exceptional employer, offering a dynamic work culture that fosters innovation and collaboration. As a Principal Statistical Programmer, you will not only contribute to cutting-edge clinical research but also benefit from extensive professional development opportunities and a supportive environment that values your expertise in R programming. Located in a vibrant area, our team enjoys a balance of meaningful work and a commitment to improving patient outcomes globally.
IQVIA

Contact Detail:

IQVIA Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Principal Statistical Programmer (R Programming)

✨Tip Number 1

Network like a pro! Reach out to your connections in the industry, especially those who work with R programming or in clinical trials. A friendly chat can lead to insider info about job openings that aren't even advertised yet.

✨Tip Number 2

Show off your skills! Create a portfolio showcasing your R packages and any projects you've worked on. This gives potential employers a taste of what you can do and sets you apart from the crowd.

✨Tip Number 3

Prepare for interviews by brushing up on common statistical programming questions and scenarios. Practice explaining your thought process when solving problems, as this will demonstrate your expertise and confidence.

✨Tip Number 4

Don't forget to apply through our website! We love seeing applications directly from candidates who are excited about joining our team. Plus, it shows you're proactive and genuinely interested in the role.

We think you need these skills to ace Principal Statistical Programmer (R Programming)

R Programming
R Shiny
Statistical Programming
Clinical Trial Analysis
Data Visualization
Data Wrangling
R Package Development
Validation of R Packages
Statistical Methodology
CDISC Data Structures
Collaboration with Statisticians
Understanding of Clinical Trial Phases
Exposure to Late Phase Studies
Real-World Evidence (RWE) Studies

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your experience in R programming and clinical trials. We want to see how your skills align with the role, so don’t be shy about showcasing relevant projects or achievements!

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about statistical programming and how you can contribute to our team. Keep it engaging and personal – we love to see your personality come through.

Showcase Your Technical Skills: When applying, make sure to mention specific R packages you've developed or validated. We’re looking for someone who can hit the ground running, so highlight any tools or methodologies you’ve used that are relevant to the role.

Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way to ensure your application gets into the right hands. Plus, you’ll find all the details you need about the role and our company culture there!

How to prepare for a job interview at IQVIA

✨Know Your R Inside Out

Make sure you brush up on your R programming skills before the interview. Be prepared to discuss your experience with developing and validating R packages, as well as any specific projects you've worked on that relate to clinical trial data. Practising coding problems or discussing your approach to statistical analysis can really help you stand out.

✨Showcase Your Collaboration Skills

Since this role involves working closely with peers and statisticians, be ready to share examples of how you've successfully collaborated in the past. Think about times when you led a project or trained team members, and be prepared to discuss how you ensured quality and accuracy in your work.

✨Understand the Bigger Picture

Familiarise yourself with the phases of clinical trials and the drug development process. Being able to articulate how your role as a Principal Statistical Programmer fits into the overall picture will demonstrate your understanding of the industry and show that you're not just focused on the technical aspects.

✨Prepare for Technical Questions

Expect to face some technical questions during the interview, especially around R and R-Shiny. Brush up on your knowledge of CDISC data structures and be ready to discuss how you've applied statistical methodologies in your previous roles. This is your chance to shine, so make sure you can confidently explain your thought process and problem-solving strategies.

Principal Statistical Programmer (R Programming)
IQVIA
Location: Looe
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