Clinical Data Programmer

ICON plc; Bengaluru; On-site; INR 900,000 - 1,300,000; Full time

Benefits offered by this job

Annual leave entitlements

Health insurance

Retirement planning

LifeWorks EAP

Life assurance

Country-specific benefits

Job summary

ICON is seeking a Clinical Data Programmer (SAS Programmer) to develop, deliver, and support data integration solutions that transform EDC data into standardized formats for downstream systems within the ARCADES ecosystem.

You will collaborate with cross-functional teams to define mapping specifications, build integrations, validate deliverables, and ensure timely delivery of subject data for full-service trials, with emphasis on Patient Data Integration (PDI) and scalable templates.

Qualifications

• 2+ years of clinical data programming or related clinical systems experience.
• SAS programming including development, testing, validation, and troubleshooting.
• Experience with raw clinical trial data, SAS datasets, and EDC exports.
• Ability to develop, review, or implement data mapping specifications.
• Understanding data transformation and system-to-system interfaces.

Responsibilities

• Develop, maintain, validate, and support Patient Data Integration (PDI) solutions for assigned studies.
• Utilize SAS programming templates to transform raw EDC data into machine-readable XML outputs.
• Review clinical trial data structures and study documentation for accurate data integration.
• Set up, monitor, and support programming deliverables and automated schedules.
• Investigate and resolve data discrepancies and integration failures.
• Perform validation and quality control to meet standards and requirements.

Skills

Analytical thinking

Problem solving

Attention to detail

Independence

Communication

Cross-functional collaboration

Education

Bachelor's degree in Computer Science, Information Systems, Life Sciences, Statistics, Mathematics, or related discipline

Tools

SAS

Medidata Rave

XML generation

Job description

Clinical Data Programmer (SAS Programmer)

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

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The Clinical Data Programmer is responsible for the development, delivery, and support of data integration solutions that transform clinical trial data collected in Electronic Data Capture (EDC) systems into standardized formats for consumption by downstream systems, including ICON's Clinical Trial Management System (CTMS), investigator payments platform, and other operational applications within the ARCADES ecosystem.

This role is primarily focused on Patient Data Integration (PDI), a core component of ICON's ARCADES platform. ARCADES leverages standardized programming frameworks, templates, and coding methodologies to transform and consolidate clinical trial data into reusable formats that support multiple downstream systems and business processes.

The Clinical Data Programmer works closely with project teams, Data Management, CTMS analysts, and other stakeholders to develop mapping specifications, build integration solutions, validate deliverables, and ensure the accurate and timely delivery of subject data for full-service clinical trials.

Key Responsibilities

Data Integration Programming & Delivery

• Develop, maintain, validate, and support Patient Data Integration (PDI) solutions for assigned studies.
• Utilize standardized SAS programming templates and frameworks to transform raw EDC data into machine-readable XML outputs.
• Review and interpret clinical trial data structures, specifications, and study documentation to ensure accurate data integration.
• Perform the setup, maintenance, monitoring, and support of programming deliverables, automated schedules, and related systems.
• Investigate, troubleshoot, and resolve programming issues, data discrepancies, and system integration failures.
• Conduct validation and quality control activities to ensure deliverables meet established standards and business requirements.

Specification Development & Collaboration

• Participate in the development and review of data mapping specifications for clinical trial integrations.
• Collaborate with project teams, CTMS analysts, Data Management, and other stakeholders to define study-specific integration requirements.
• Translate approved mapping specifications and business rules into programming solutions.
• Review visit mappings, attribute mappings, and integration logic to ensure alignment between source and target systems.
• Provide input on integration design, feasibility, and implementation approaches during study startup and maintenance activities.

Team Support & Quality

• Participate in peer review and quality control activities to ensure high-quality programming deliverables.
• Share technical knowledge and best practices with other Clinical Data Programmers.
• Provide support and guidance to less experienced team members as appropriate.
• Work collaboratively with team members to meet departmental objectives and project timelines.
• Support the Clinical Data Programming Lead and contribute to team initiatives as required.

Required Experience & Qualifications

Experience

• 2+ years of experience in clinical data programming, clinical data integration, or a related clinical systems role.
• SAS programming experience, including development, testing, validation, and troubleshooting.
• Experience working with raw clinical trial data, including SAS datasets and EDC exports.
• Experience developing, reviewing, or implementing data mapping specifications.
• Understanding of data transformation, data integration, and system-to-system interfaces.
• Ability to manage multiple studies, priorities, and timelines simultaneously.
• Strong analytical and problem-solving skills with the ability to investigate complex data issues.
• Experience participating in quality review, validation, and testing activities.
• Experience contributing to process improvement, standardization, or automation initiatives.

Preferred Experience

• Experience with Medidata Rave and/or other leading EDC systems.
• Experience supporting integrations between clinical systems.
• Familiarity with XML generation and structured data exchange methodologies.

Key Competencies

• Strong technical and analytical skills.
• Excellent attention to detail and commitment to quality.
• Strong problem-solving and troubleshooting abilities.
• Ability to work independently with minimal supervision.
• Effective verbal and written communication skills.
• Ability to collaborate across multiple functional groups and stakeholders.
• Strong learning agility and willingness to adopt new technologies and processes.
• Commitment to continuous improvement and operational excellence.

Education

Bachelor's degree in Computer Science, Information Systems, Life Sciences, Statistics, Mathematics, or a related discipline, or equivalent relevant experience.

What ICON can offer you:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs.
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here