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Senior Clinical Data Science Programmer

6+ years
Not Disclosed
10 Nov. 12, 2025
Job Description
Job Type: Full Time Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ 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

Location: India (Remote)
Job ID: 2025-121459
Department: ICON Strategic Solutions – Biometrics Portfolio
Employment Type: Full-Time (Remote)


About ICON

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment that drives innovation and excellence. Join us on our mission to shape the future of clinical development and make a meaningful impact on global health.


Position Overview

The Senior Clinical Data Science Programmer will play a key role in the design, development, and validation of clinical trials within Electronic Data Capture (EDC) systems. This position involves leading programming activities, managing system configurations, and ensuring data integrity across studies. The ideal candidate will have strong EDC programming expertise and the ability to integrate multiple clinical systems efficiently.


Key Responsibilities

  • Design, develop, and validate clinical trials in EDC systems.

  • Manage edit check specifications and configure edit checks at the trial level.

  • Execute User Acceptance Testing (UAT) scripts to validate study setup.

  • Configure and manage study instances (UAT, production, testing).

  • Facilitate user access requests for study teams and manage user roles.

  • Oversee blinded and unblinded study configurations in EDC.

  • Serve as the Subject Matter Expert (SME) for all trial-level EDC database activities.

  • Configure, validate, and integrate other modules within the EDC ecosystem such as coding, IRT, safety systems, and lab integrations.

  • Troubleshoot database setup and implement post-production updates.

  • Conduct impact assessments for post-production changes and ensure validation.

  • Support adoption of new technologies and process improvements.

  • Lead vendor oversight and coordinate with technology vendors and CRO partners.

  • Ensure TMF (Trial Master File) documentation is archived and inspection-ready.

  • Prepare for regulatory inspections or audits, representing the Clinical Trial Configuration Group.


Required Qualifications & Skills

  • Education: Bachelor’s degree in Life Sciences, Computer Science, Data Science, or related field.

  • Experience:

    • Minimum 6+ years in Clinical Data Management, Clinical Programming, or related roles.

    • At least 4 years’ experience in EDC programming.

  • Technical Skills:

    • Hands-on experience with Veeva (mandatory), Medidata Rave, or Oracle Inform.

    • Knowledge of CQL, CDB, JSON, and/or C# preferred.

    • Experience integrating EDC systems with lab, safety, IRT, and coding modules.

    • Understanding of CTMS, SAS, R, Python, Data Warehouses, and SharePoint.

  • Knowledge: Solid understanding of the drug development process and GCP standards.

  • Soft Skills: Strong problem-solving ability, attention to detail, and excellent communication and coordination skills.


Experience Level

  • Mid to Senior Level

  • Typically 6–9 years of total experience in Clinical Data Management or Clinical Programming.

  • Demonstrated leadership in EDC programming and system integration.


Job Category

  • Primary Category: Clinical Data Science / Clinical Programming

  • Subcategories:

    • EDC Programming and Configuration

    • Data Management and System Integration

    • Clinical Research Technology Operations


What ICON Can Offer You

ICON’s success depends on the quality of its people. We foster a diverse culture that rewards excellence and supports growth and work-life balance.

Benefits Include:

  • Competitive annual leave entitlements.

  • Comprehensive health insurance options for you and your family.

  • Retirement and savings plans to help plan your future with confidence.

  • Global Employee Assistance Programme (TELUS Health) — 24/7 support for personal well-being.

  • Life assurance and flexible, country-specific optional benefits such as:

    • Childcare vouchers

    • Bike purchase schemes

    • Discounted gym memberships

    • Subsidized travel passes

    • Health assessments