[Hiring] Principal Clinical Data Standards Consultant - R Programmer @ICON plc

Role Description

The Global Data Standards team is seeking an experienced and innovative Principal Clinical Data Standards Consultant to help drive the evolution of clinical data standards, standards-enabled technologies, and R-based solutions across the organization. This role offers the opportunity to influence enterprise-wide standards strategy, shape the future of R adoption, and lead the development of scalable solutions that improve efficiency, quality, and regulatory compliance across clinical development programs.

• Develop, implement, and maintain ICON SDTM and ADaM standards libraries from data collection through analysis and submission.
• Support sponsors in the development, implementation, maintenance, and governance of clinical data standards content.
• Provide internal and external consulting on SDTM compliance, standards implementation, and industry best practices.
• Participate in standards governance team meetings and provide standards input as assigned.
• Support the 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 CDISC 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, with a specific focus on SDTM 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 the 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.

Qualifications

• Minimum of 8 years of experience in clinical trials programming, data standards management, or a related clinical data science discipline.
• Advanced expertise in CDISC SDTM standards, including implementation, governance, compliance, and regulatory submission requirements.
• Working knowledge of ADaM standards and standards development across the clinical data lifecycle a plus.
• Advanced proficiency in R programming.
• Hands-on R Shiny development experience, particularly for dashboards or data-driven applications a plus.
• Demonstrated ability to lead technical initiatives and influence cross-functional stakeholders.
• Excellent communication, consulting, mentoring, and problem-solving skills.

Requirements

• Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Benefits

• Competitive base salary and performance related incentives.
• Health and wellbeing programmes including medical, dental, and vision coverage where applicable.
• Retirement and pension plans.
• Life assurance and disability coverage.
• Employee assistance programmes and wellbeing resources.
• Learning and development opportunities through structured training and career pathways.
• Benefits may vary depending on role and location.