Strong experience in r programming for clinical trials
Developing and validating r packages from cro or pharma
Advanced knowledge of cdisc data structures
IQVIA is seeking an R Programming Lead to join their sponsor-dedicated team, focusing on the development and validation of R packages for clinical trial analysis. The ideal candidate should have extensive experience in R programming, particularly in the context of clinical trials, and a strong understanding of statistical methodologies
Job Summary
Join a sponsor-dedicated team to advance in-house study activities by providing technical expertise as an R Programming Lead.
You will be responsible for developing internal and external R packages for clinical trial analysis including ADaM, tables, figures, and listings.
The role involves leading implementation in R, training Biostatistics team members, and creating global tools to increase efficiency.
Matching Summary
Match Score: 85
IQVIA is seeking an R Programming Lead to join their sponsor-dedicated team, focusing on the development and validation of R packages for clinical trial analysis. The ideal candidate should have extensive experience in R programming, particularly in the context of clinical trials, and a strong understanding of statistical methodologies.
Skills & Requirements
Must-have
Strong experience in R programming for clinical trials
Developing and validating R packages from CRO or Pharma
Advanced knowledge of CDISC data structures
Creating safety and efficacy study outputs like ADaM
Building complex R-Shiny applications for dashboards
Nice-to-have
Exposure to Late Phase Real-World Evidence studies
Experience with Global Medical Affairs studies
Ability to reproduce statistical analysis using R
Key Requirements
Strong experience in R programming for clinical trial data
Proven experience applying R and R-Shiny for clinical trial analysis
Advanced knowledge of industry standards including CDISC data structures