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ICON plc

Principal Statistical Programmer

ICON plc

. Manage day-to-day statistical programming activities, supporting the team to deliver quality outcomes .

Posted 11/5/2026full-timeRemote • China, TaiwanLeadWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in statistical programming, particularly with SAS, R, or Python, while ensuring compliance with regulatory standards in clinical trials. Provides mentorship to junior programmers and collaborates effectively with biostatisticians and clinical teams to achieve project objectives.

Highest-signal resume keywords
Statistical ProgrammingSASRPythonRegulatory Submissions

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Statistical AnalysisData ManagementProgramming SpecificationsTechnical ReportingQuality Assurance
Soft Skills
Problem-SolvingAttention to DetailCommunicationInterpersonal SkillsMentorship
Industry Keywords
Clinical TrialsRegulatory StandardsBiostatisticsData AnalysisStatistical Programming Activities

Tech Stack

Tools & technologies
Python

About the role

Key responsibilities & impact
  • Manage day-to-day statistical programming activities, supporting the team to deliver quality outcomes
  • Lead the development and validation of statistical programs for data analysis and reporting, ensuring compliance with regulatory standards
  • Collaborate with biostatisticians and clinical teams to define project requirements and align with study objectives
  • Oversee the creation of programming specifications, documentation, and technical reports for regulatory submissions
  • Provide mentorship and guidance to junior statistical programmers
  • Stay current with industry trends and advancements in statistical programming to drive innovation and enhance project outcomes

Requirements

What you’ll need
  • Bachelor's degree in statistics, computer science, mathematics, or a related discipline
  • Significant experience in statistical programming, particularly in the context of clinical trials and regulatory submissions
  • Expertise in programming languages such as SAS, R, or Python, with proficiency in data management and statistical analysis
  • Excellent problem-solving skills and attention to detail, with a commitment to delivering high-quality results
  • Strong communication and interpersonal skills, facilitating effective collaboration across teams and with stakeholders
  • A commitment to maintaining high standards of quality and compliance in all programming activities
  • Legal right to work in the country where the role is based

Benefits

Comp & perks
  • 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