R Programming Lead

IQVIA; Reading; On-site; GBP 50,000 - 85,000; Full time

Job summary

IQVIA seeks an R Programming Lead in Reading, England. This role involves overseeing the Statistical Programming team, developing R packages, and ensuring high-quality solutions for clinical trials. Ideal candidates will have extensive experience in R programming, data visualization, and statistical methodologies within the pharmaceutical industry. Join a leader in advancing healthcare outcomes worldwide.

Qualifications

• Strong skills in developing and validating R packages.
• Proven experience in statistical analysis and reporting.

Responsibilities

• Develop internal and external R packages for clinical trials.
• Ensure the quality and accuracy of clinical data for submission.
• Train Biostatistics team members on R and package implementation.

Skills

Strong programming skills in R/R Shiny

Data visualization skills

Data wrangling skills

Education

Minimum 5+ years experience in R programming

Job description

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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.
• 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.
• 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

Seniority level

• Seniority level

  Not Applicable

Employment type

• Employment type

  Full-time

Job function

• Job function

  Other

• Industries

  Pharmaceutical Manufacturing

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