R Programming Lead

IQVIA Argentina; Reading; On-site; GBP 50,000 - 75,000; Full time

Job summary

A global clinical research organization in Reading seeks an experienced R Programming Lead to enhance in-house study activities. The role involves developing R packages for clinical trials, conducting statistical programming, and training team members. Candidates should have over 5 years of experience, strong skills in R and R Shiny, and expertise in clinical trial analysis. Competitive salary and benefits offered.

Qualifications

• Minimum 5+ years of experience in R programming for clinical trial data.
• Strong programming skills in R/R Shiny.
• Proven ability to apply R for analysis and reporting of clinical trials.
• Experience with industry standards including CDISC data structures.

Responsibilities

• Develop internal and external R packages for clinical trial analysis.
• Lead implementation in R and train Biostatistics team members.
• Conduct statistical programming work of clinical data using R.
• Create and validate safety and efficacy study outputs consistent with study documentation.

Skills

R programming

Data visualization

Data wrangling

R Shiny

Statistical analysis

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

• 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