Associate Director, R & Shiny Analytics

Daiichi Sankyo US

Basking Ridge (NJ)

On-site

USD 171,000 - 257,000

Full time

7 days ago
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Job summary

Daiichi Sankyo US seeks a senior Statistical Programmer to provide expert support for R programming, develop R packages and Shiny apps, and lead R programming implementations across studies.

You will collaborate with cross-functional teams, serve as R SME, guide development, and contribute to data surveillance and safety signaling with advanced statistics and CDISC SDTM/ADaM knowledge.

Qualifications

  • Bachelor's Degree in a science or technical field such as computer science or mathematics required; Master's Degree preferred.
  • 10+ years of experience with R programming and Shiny app development in clinical trials.
  • Advanced working knowledge of R and SAS in clinical trials programming.
  • CDISC SDTM and ADaM implementation experience in clinical trials analysis.
  • Strong understanding of statistical concepts for analyses and reporting in clinical trials.
  • Knowledge of all phases of drug development and applied statistics.
  • Solid knowledge of new advanced statistical methods using SAS or R.
  • Advanced database knowledge and setup.

Responsibilities

  • Lead and contribute to DS R programming system development and strategy for R shiny apps.
  • Provide technical guidance and act as R programming SME for internal/external collaborations.
  • Lead UATs and resolve R programming issues across projects.
  • Develop and validate R packages and shiny apps and publish study-specific apps.
  • Collaborate with cross-functional teams to enable data surveillance and safety signaling.

Skills

R programming
Shiny app dev
CDISC SDTM/ADaM
SAS programming
Statistics concepts
Clinical trials
Drug development
Data surveillance

Education

Bachelor's degree in science/tech

Tools

SAS

Job description

Daiichi Sankyo US seeks a senior Statistical Programmer to provide expert support for R programming, develop R packages and Shiny apps, and lead R programming implementations across studies.

You will collaborate with cross-functional teams, serve as R SME, guide development, and contribute to data surveillance and safety signaling with advanced statistics and CDISC SDTM/ADaM knowledge.

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