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Statistical Programmer

Icon Plc
ICON PLC
5+ years
Not Disclosed
10 Jan. 22, 2026
Job Description
Job Type: Full Time Remote Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Statistical Programmer II – Bangalore
Location: Bangalore, Karnataka, India
Employment Type: Full-time
Job ID: JR139820
Work Mode: Office or Home-based


About ICON

ICON plc is a global leader in healthcare intelligence and clinical research services, providing innovative solutions that advance clinical development. We foster an inclusive, collaborative, and high-performing culture that empowers employees to make an impact in clinical trials worldwide.


Role Overview

As a Statistical Programmer II, you will develop, validate, and execute statistical programs for clinical trial analysis and reporting, ensuring the accurate interpretation of study data. You will collaborate closely with biostatisticians and cross-functional teams to deliver high-quality statistical outputs that comply with industry standards and regulatory guidelines.

This role is ideal for professionals with strong statistical programming expertise and experience in clinical research, looking to contribute to critical clinical trial deliverables while mentoring junior team members.


Key Responsibilities

  • Develop, validate, and maintain complex statistical programs (SAS, R, or Python) for data manipulation, analysis, and reporting.

  • Collaborate with biostatisticians and cross-functional teams to implement study-specific statistical analyses accurately.

  • Prepare and review Statistical Analysis Plans (SAPs), programming specifications, and derived datasets.

  • Ensure data integrity and compliance with regulatory standards, including ICH-GCP guidelines.

  • Mentor and train junior programmers, promoting best practices and technical development within the team.

  • Contribute to process improvement and standardization of statistical programming practices.


Qualifications & Skills

  • Bachelor’s degree in Statistics, Mathematics, Computer Science, or related field; advanced degree preferred.

  • 5+ years of experience as a statistical programmer in clinical research.

  • Proficiency in SAS, R, or Python, and experience with clinical data management systems.

  • Strong analytical and problem-solving skills with attention to detail.

  • Excellent communication skills for collaboration across technical and non-technical teams.


Why Join ICON

  • Be part of a global clinical research leader shaping the future of healthcare.

  • Competitive salary and comprehensive benefits, including health insurance, retirement plans, and flexible work options.

  • Opportunities for career growth, mentoring, and professional development.

  • Inclusive culture that values diversity, equity, and belonging.