Not specified (assumed to be hybrid or onsite based on the nature of the role).
Strong experience in r programming for clinical trials
Developing and validating r packages
Building complex r-shiny applications
IQVIA UK is seeking a Principal Statistical Programmer with expertise in R programming for clinical trial data analysis. The role involves developing and validating R packages, creating R-Shiny applications, and ensuring data integrity throughout various project phases
Job Summary
The role involves developing internal and external R packages specifically for clinical trial analysis including ADaM, tables, figures, and listings.
Candidates will lead the implementation of R tools and train Biostatistics team members to increase group efficiency.
The position requires ensuring submission readiness of clinical data consistent with Health Authority requirements and industry standards.
Matching Summary
Match Score: 85
IQVIA UK is seeking a Principal Statistical Programmer with expertise in R programming for clinical trial data analysis. The role involves developing and validating R packages, creating R-Shiny applications, and ensuring data integrity throughout various project phases.
Salary
Base: $69,300.00 - $173,200.00 annualized; Bonus/Equity: Dependent on position offered; Benefits: Range of health and welfare benefits included
Skills & Requirements
Must-have
Strong experience in R programming for clinical trials
Developing and validating R packages
Building complex R-Shiny applications
Creating ADaM tables figures listings
Knowledge of CDISC data structures
Nice-to-have
Experience with Real-World Evidence studies
Exposure to Late Phase studies
Global Medical Affairs study experience
Ability to train other team members
Key Requirements
Strong experience in R programming from CRO or Pharmaceutical Industry
Advanced knowledge of CDISC data structures
Proven ability to reproduce statistical analysis using R