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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.
Strong understanding of end-to-end Clinical Trials in Statistical Programming is mandatory.
Exposure to Late Phase & Real-World Evidence (RWE) studies is highly desirable.
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, including 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.
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
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Data Scientist • Dublin, Ireland