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ICON plc

Statistical Programmer

ICON plc

. Develop, validate, and maintain statistical programs (SAS, R, or similar) for data manipulation, analysis, and reporting in clinical trials .

Posted 10/5/2026full-timeTokyo • JapanMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in statistical programming using SAS, R, or Python, with a strong focus on data integrity and compliance with ICH/GCP guidelines in clinical trials. Capable of collaborating effectively with biostatisticians and clinical teams to deliver high-quality statistical analyses and documentation.

Highest-signal resume keywords
Statistical Programming (SAS, R, Python)Clinical Data Management SystemsStatistical Analysis Plans (SAPs)ICH/GCP ComplianceAnalytical and Problem-Solving Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Statistical ProgrammingData ManipulationData AnalysisStatistical MethodologiesProgramming SpecificationsClinical Study ReportsRegulatory StandardsData IntegrityStatistical Analysis PlansClinical Trials
Soft Skills
Attention to DetailTeam CollaborationCommunication Skills
Tools & Technologies
SASRPythonClinical Data Management Systems
Industry Keywords
Clinical ResearchICH GuidelinesGCP Guidelines

Tech Stack

Tools & technologies
Python

About the role

Key responsibilities & impact
  • Develop, validate, and maintain statistical programs (SAS, R, or similar) for data manipulation, analysis, and reporting in clinical trials
  • Collaborate with biostatisticians and clinical teams to understand project requirements and ensure accurate implementation of statistical analyses
  • Prepare and review statistical analysis plans (SAPs) and programming specifications to meet regulatory standards
  • Ensure data integrity and compliance with industry regulations, including ICH/GCP guidelines, throughout the programming process
  • Participate in the preparation of clinical study reports and other documentation required by regulatory authorities
  • Deliver statistical programming work to a high standard while working closely with team members and stakeholders

Requirements

What you’ll need
  • Bachelor's degree in statistics, computer science, mathematics, or a related discipline
  • Proven experience as a statistical programmer within the clinical research industry, with strong knowledge of statistical methodologies
  • Proficiency in programming languages such as SAS, R, or Python, along with experience in clinical data management systems
  • Strong analytical and problem-solving skills, with attention to detail and the ability to work independently and as part of a team
  • Excellent communication skills, with the ability to convey complex statistical concepts to non-technical stakeholders
  • 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