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Senior Clinical Data Science Programmer

Icon Plc
ICON PLC
0-2 years
Not Disclosed
10 Jan. 22, 2026
Job Description
Job Type: Full Time Hybrid 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: Senior Clinical Data Science Programmer – Chennai/Bangalore
Location: Chennai, Tamil Nadu, India | Bangalore, Karnataka, India
Employment Type: Full-time
Work Mode: Office with Flexibility
Job ID: JR141859


About ICON

ICON plc is a world-leading healthcare intelligence and clinical research organization, delivering innovative solutions that advance clinical development globally. We foster an inclusive, collaborative environment where talent thrives and data-driven insights support cutting-edge therapies.


Role Overview

We are seeking a Senior Clinical Data Science Programmer to develop, validate, and implement advanced programming solutions that support the analysis and reporting of clinical trial data. You will work closely with clinical data scientists, biostatisticians, and cross-functional teams to ensure data accuracy, operational efficiency, and regulatory compliance in clinical research.


Key Responsibilities

  • Develop, validate, and maintain programming solutions for clinical trial data analysis and reporting.

  • Collaborate with clinical data scientists and biostatisticians to integrate programming solutions into overall data management workflows.

  • Oversee generation of statistical datasets, tables, listings, and figures for regulatory submissions and study reports.

  • Provide guidance on programming best practices, coding standards, and data quality control measures.

  • Stay current with advancements in programming languages and clinical data tools to enhance efficiency and innovation.

  • Mentor junior programmers and contribute to the development of programming standards and knowledge-sharing initiatives.


Qualifications & Skills

  • Advanced degree in Computer Science, Statistics, Life Sciences, or a related field.

  • Extensive experience in clinical trial programming, with proficiency in SAS, R, or Python.

  • Strong problem-solving skills, with the ability to work collaboratively in a fast-paced, cross-functional environment.

  • Exceptional attention to detail and organizational skills, ensuring high-quality deliverables.

  • Excellent communication and interpersonal skills, with the ability to influence and work effectively with diverse teams.


Why Join ICON

  • Global impact: Contribute to innovative clinical research advancing therapies worldwide.

  • Comprehensive benefits: Health insurance, retirement plans, flexible work options, life assurance, and wellness programs.

  • Career growth: Mentorship, training programs, and opportunities to advance within clinical data and programming disciplines.

  • Inclusive culture: ICON values diversity, equity, and belonging in all aspects of its operations.