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IQVIA

R Programming Lead (Statistical Programming) m/w/d

Reposted 17 Days Ago
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7 Locations
Senior level
7 Locations
Senior level
Lead the technical aspects of statistical programming for clinical trial analysis using R. Responsibilities include developing and validating R packages, conducting statistical programming, collaborating with statisticians, and ensuring quality and accuracy of clinical data outputs. Requires strong knowledge in ADaM, SDTM, CDISC, and experience in pharmaceutical clinical development.
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Join a sponsor-dedicated team, progressing with in-house study activities over the years. Experienced R programmer needed to provide technical expertise for Statistical Programming Team to meet internal and external needs.

• 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.
• Identifies problems and develops 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)
• Collaborates with peers and statisticians to ensure the quality and accuracy –thus submission readiness –of clinical data as required by authorities (i.e. 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.
  • 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.

In-depth understanding of the phases of clinical trials and the drug development process. Experience in late-phase (Phase IV) clinical trials and Real-World Evidence (RWE) 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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