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ICON plc

Statistical Programmer II

ICON plc

. Develop, validate, and maintain complex statistical programs for data manipulation, analysis, and reporting in clinical trials .

Posted 9/18/2026full-timeRemote • IndiaMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in statistical programming for clinical trials, including proficiency in SAS, R, and Python, while ensuring compliance with ICH/GCP guidelines. Capable of mentoring junior programmers and collaborating effectively with cross-functional teams to deliver high-quality statistical analyses.

Highest-signal resume keywords
Statistical ProgrammingSASRPythonClinical Data Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Statistical ProgrammingData ManipulationStatistical AnalysisProgramming SpecificationsStatistical Analysis PlansData IntegrityRegulatory ComplianceStatistical MethodologiesClinical TrialsData Reporting
Soft Skills
Analytical SkillsProblem-Solving SkillsAttention to DetailCommunication SkillsCollaboration
Tools & Technologies
Clinical Data Management Systems
Industry Keywords
ICH GuidelinesGCP GuidelinesClinical ResearchStatistical Programming Deliverables

Tech Stack

Tools & technologies
Python

About the role

Key responsibilities & impact
  • Develop, validate, and maintain complex statistical programs for data manipulation, analysis, and reporting in clinical trials
  • Collaborate with biostatisticians and cross-functional teams to interpret study requirements and implement statistical analyses accurately
  • Prepare and review statistical analysis plans, programming specifications, and derived datasets to meet regulatory standards
  • Ensure data integrity and compliance with industry regulations, including ICH/GCP guidelines
  • Mentor junior programmers and assist in training team members on programming techniques and best practices
  • Take responsibility for statistical programming deliverables in a sponsor-dedicated model

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 and programming
  • Proficiency in programming languages such as SAS, R, or Python, with experience in clinical data management systems
  • Strong analytical and problem-solving skills, with a keen attention to detail and the ability to work independently
  • Excellent communication skills, with the ability to convey complex statistical concepts to non-technical stakeholders and collaborate effectively with team members
  • 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