R Programming Lead

Nanosep AB; Reading; On-site; GBP 60,000 - 80,000; Full time

Job summary

A leading company is seeking an R Programming Lead to join their Statistical Programming team. The role involves developing and validating R packages for clinical trials, ensuring high-quality solutions, and collaborating with statisticians. Candidates should have over 5 years of experience in R programming, strong skills in data visualization, and a solid understanding of clinical trial processes.

Qualifications

• Minimum 5+ years of experience in R programming for clinical trial data.
• Strong programming skills in R/R Shiny.
• Proven experience in applying R for analysis and reporting of clinical trials.

Responsibilities

• Develop internal and external R packages for clinical trial analysis.
• Lead implementation in R and train other Biostatistics team members.
• Collaborate with peers and statisticians to ensure quality of clinical data.

Skills

R programming

Data visualization

Data wrangling

Statistical methodology

R Shiny

Job description

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

1. Develop internal and external R packages for clinical trial analysis (ADaM, tables, figures, listings).
2. Validate R packages.
3. Lead implementation in R and train other Biostatistics team members.
4. Conduct statistical programming work of clinical data using R.
5. Identify problems and develop global tools to increase the efficiency and capacity of the Statistical Programming group.
6. Create and validate safety and efficacy study output requirements (e.g., ADaM, TLFs) consistent with data definitions, specifications, and relevant documentation (e.g., protocol, SAP, aCRF).
7. Collaborate with peers and statisticians to ensure the quality and accuracy of clinical data for submission readiness (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 analysis and reporting of clinical trials, with the ability to reproduce statistical analyses using R.
• Strong skills in data visualization and data wrangling using R, with proficiency in R packages for data exploration and visualization.
• Application of statistical methodology and concepts in clinical trial analysis, with experience in R-Shiny apps for data exploration.
• Advanced knowledge of industry standards including CDISC data structures, and a solid understanding of the development and use of standard programs.
• In-depth understanding of clinical trial phases 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 connections that accelerate the development and commercialization of innovative medical treatments. Learn more at https://jobs.iqvia.com.

IQVIA is committed to diversity and inclusion. We seek talented individuals with curious minds and a commitment to innovation and impact. Everyone at IQVIA contributes to our shared goal of improving patient outcomes and population health worldwide.

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