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Global drug and device development services

Principal Clinical Data Standards Consultant - R Programmer

Quantitative Biology & BiostatisticsConfirmed live in the last 24 hours
Full-time

About the Job

Requirements

  • A minimum of 8 years of experience in clinical trials programming, data standards management, or a related clinical data science discipline is required.
  • Advanced expertise in Clinical Data Interchange Standards Consortium Study Data Tabulation Model standards, including implementation, governance, compliance, and regulatory submission requirements, is required.
  • Advanced proficiency in R programming is required.
  • The role requires the ability to lead technical initiatives and influence cross-functional stakeholders.
  • The role requires communication, consulting, mentoring, and problem-solving skills.

Responsibilities

  • Develop, implement, and maintain ICON Study Data Tabulation Model and Analysis Data Model standards libraries from data collection through analysis and submission.
  • Support sponsors in developing, implementing, maintaining, and governing clinical data standards content.
  • Provide internal and external consulting on Study Data Tabulation Model compliance, standards implementation, and industry best practices.
  • Participate in standards governance team meetings and provide standards input as assigned.
  • Support development and maintenance of technologies used to implement and manage clinical data standards.
  • Design and implement standardized programming frameworks for clinical reporting, analysis, and submission deliverables.
  • Develop and deliver training on Clinical Data Interchange Standards Consortium standards-related topics for internal teams and external sponsors.
  • Provide expert guidance and hands-on support for study-specific R programming activities.
  • Develop and maintain reusable R packages, functions, utilities, and automation tools, focusing on Study Data Tabulation Model processes and deliverables.
  • Design and develop R Shiny applications to support dashboards and a Data Monitoring Committee initiative.
  • Perform code reviews and establish best practices to ensure quality, consistency, scalability, and compliance.
  • Partner with the R Business Solutions Organization to advise on R adoption strategy and roadmap.
  • Drive development of scalable templates, workflows, and governance models that support enterprise-wide R adoption.
  • Contribute to departmental technology strategy and help shape future programming capabilities.
  • Mentor and coach programmers and statisticians transitioning to R.
  • Support onboarding and enablement activities for new R users.

Desired Qualifications

  • Working knowledge of Analysis Data Model standards and standards development across the clinical data lifecycle is a plus.
  • Hands-on R Shiny development experience, particularly for dashboards or data-driven applications, is a plus.

About the Company

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Global drug and device development services

This company provides consulting, development, and commercialization support for drugs and medical devices through a global network of offices. Its team across 53 countries offers end-to-end services, from strategy and regulatory work to manufacturing and market access, helping clients shorten development time, lower costs, and raise quality. It differentiates itself with wide geographic reach and a clear focus on reducing time to market and cost while leveraging deep experience across many therapeutic areas. Its goal is to help clients accelerate the development of life-saving products and improve quality of life by delivering reliable information, practical solutions, and solid performance.

Company size
10,001+
Company stage
IPO
Headquarters
Ireland
Founded
1990

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