Senior Clinical Data Science Programmer
Company: ICON plc
Locations: Bangalore / Chennai / Trivandrum, India
Work Mode: Office with Flex (Hybrid)
Department: Clinical Data Science / Clinical Data Management
Employment Type: Full-Time
Experience: 5+ years of experience in Clinical Data Programming or Statistical Programming within the Clinical Research or CRO industry, with expertise in SAS, R, Python, Medidata Rave Custom Functions, and Clinical SAS Listings.
Salary Package: ₹18–28 LPA (Approx., based on current market standards; final compensation depends on candidate experience, programming expertise, and clinical trial exposure.)
Role Overview
The Senior Clinical Data Science Programmer is responsible for developing, validating, and implementing programming solutions that support clinical trial data analysis, reporting, and data management. The role collaborates closely with Clinical Data Scientists, Biostatisticians, and cross-functional teams to ensure high-quality programming deliverables, regulatory compliance, and efficient processing of clinical trial data.
Key Responsibilities
Clinical Data Programming
Develop, validate, and maintain programming code to support clinical trial data analysis and reporting.
Create efficient programming solutions for processing and transforming clinical trial data.
Generate Clinical SAS Listings and other programming deliverables.
Ensure programming outputs are accurate, validated, and completed within project timelines.
Statistical Programming & Data Analysis
Collaborate with Clinical Data Scientists and Biostatisticians to understand study requirements and analytical objectives.
Support statistical analyses by preparing analysis datasets and programming outputs.
Review analysis datasets and final reports to ensure accuracy, consistency, and completeness.
Contribute to data analysis and reporting activities across clinical studies.
Programming Documentation & Validation
Create and maintain programming documentation, including:
Programming specifications
Validation documentation
Code documentation
Output documentation
Perform programming validation to ensure data quality and integrity.
Maintain version control and documentation standards.
Regulatory Compliance & Quality
Ensure compliance with:
ICH-GCP Guidelines
Regulatory requirements
Company SOPs
Industry programming standards
Maintain high standards of data integrity throughout the programming lifecycle.
Support audit and inspection readiness by ensuring complete and accurate documentation.
Cross-Functional Collaboration
Work closely with:
Clinical Data Science
Biostatistics
Clinical Data Management
Clinical Operations
Medical Writing
Participate in project discussions and provide programming expertise.
Communicate technical programming concepts effectively to cross-functional teams.
Support timely delivery of clinical trial milestones.
Continuous Improvement
Contribute to programming process improvements and standardization initiatives.
Promote programming best practices and quality standards.
Support knowledge sharing within the programming team.
Assist in improving programming efficiency through automation where applicable.
Educational Qualification
Bachelor's degree in:
Computer Science
Statistics
Life Sciences
Data Science
Or another related discipline
Required Experience
Minimum 5 years of experience in Clinical Data Programming or Statistical Programming within the Clinical Research, Pharmaceutical, Biotechnology, or CRO industry.
Hands-on experience supporting clinical trial data analysis and reporting.
Experience creating Clinical SAS Listings.
Experience collaborating with Clinical Data Science and Biostatistics teams.
Technical Skills
Strong proficiency in:
SAS
R
Python
Medidata Rave (Custom Functions)
Experience with:
Clinical SAS Listings
Clinical trial data processing
Statistical programming
Data validation
Analysis datasets
Good understanding of Clinical Data Management processes.
Knowledge of ICH-GCP guidelines and global regulatory requirements.
Proficiency in Microsoft Office applications.
Key Competencies
Strong programming and analytical skills.
Excellent problem-solving and logical thinking abilities.
High attention to detail and data accuracy.
Strong communication and collaboration skills.
Ability to work independently and manage multiple projects.
Excellent organizational and documentation skills.
Commitment to quality, compliance, and continuous improvement.
Ability to deliver high-quality programming outputs within project timelines.
Uttar Pradesh :
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Remote, India | Siliguri |Illinois :
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