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Statistical Programmers

Icon Plc
ICON PLC
0-2 years
Not Disclosed
10 Jan. 22, 2026
Job Description
Job Type: Full Time 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 / Senior Statistical Programmer – Trivandrum / Chennai
Location: Trivandrum, Kerala, India | Chennai, Tamil Nadu, India
Employment Type: Full-time
Work Mode: Office or Home
Job ID: JR142451


About ICON

ICON plc is a global leader in healthcare intelligence and clinical research, committed to advancing clinical development through innovation, inclusivity, and operational excellence. We deliver high-quality programming and data solutions that support clinical trials, regulatory submissions, and ultimately patient outcomes.


Role Overview

ICON is hiring Statistical Programmers II and Senior Statistical Programmers to develop, validate, and deliver statistical programming solutions for clinical trial data analysis and reporting. These roles provide critical support to biostatisticians and cross-functional teams, ensuring compliance with regulatory standards and maintaining the highest data quality.


Key Responsibilities

  • Develop, validate, and maintain statistical programs for clinical trial data analysis using R, R Shiny, and SAS.

  • Collaborate with biostatisticians to interpret study requirements and implement statistical analysis plans accurately.

  • Prepare and review programming specifications, derived datasets, and outputs in line with regulatory standards (ICH/GCP).

  • Perform quality control checks to ensure data integrity, accuracy, and consistency across all deliverables.

  • Support the preparation of statistical reports, tables, listings, and figures for regulatory submissions and internal stakeholders.

  • Contribute to process improvements and best practices within the statistical programming function.

  • For senior programmers: mentor junior staff, facilitate knowledge sharing, and support team development initiatives.


Candidate Profile

  • Degree in Statistics, Mathematics, Computer Science, or related discipline (advanced degree preferred).

  • Hands-on experience in statistical programming within clinical research or pharmaceutical environments.

  • Proficiency in R, R Shiny, and SAS; solid understanding of statistical methodologies and clinical trial data.

  • Knowledge of regulatory requirements, including ICH/GCP guidelines.

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

  • Effective communication skills for collaboration with technical and non-technical stakeholders.

  • Flexible opportunity for varying levels of experience, with potential for career growth and skill development.


Why Join ICON

  • Global Impact: Contribute to meaningful clinical research supporting innovative therapies.

  • Career Growth: Mentorship, training, and advancement opportunities within statistical programming.

  • Comprehensive Benefits: Health insurance, retirement planning, flexible work options, life assurance, wellness programs.

  • Inclusive Culture: ICON values diversity, equity, and belonging, fostering a supportive and engaging workplace.