Clinical Data Science Programmer
Locations: Bengaluru, Chennai, Trivandrum, India
Work Model: Office with Flex (Hybrid)
Employment Type: Full-Time
Posted: 6 Days Ago
Job Requisition ID: JR139875
Company: ICON plc
About ICON plc
ICON plc is a globally recognized healthcare intelligence and clinical research organization supporting pharmaceutical, biotechnology, and medical device companies in delivering innovative therapies to patients worldwide. ICON is known for its scientific excellence, regulatory expertise, and commitment to diversity, innovation, and career growth.
Position Overview
ICON is seeking a Clinical Data Science Programmer to support the development and implementation of advanced programming solutions for clinical trial data analysis. This role is integral to ensuring data accuracy, regulatory compliance, and efficient delivery of statistical outputs that support critical clinical research and regulatory submissions.
The successful candidate will collaborate closely with clinical data scientists, statisticians, and cross-functional teams to translate clinical data requirements into high-quality, validated programming solutions.
Key Responsibilities
Develop, validate, and maintain statistical programming code to support clinical trial data analysis and reporting
Collaborate with data scientists, statisticians, and clinical teams to understand analytical requirements and data specifications
Ensure programming activities comply with ICH-GCP guidelines, regulatory standards, and internal SOPs
Create and maintain comprehensive documentation for programming processes, code development, and outputs
Participate in the review of analysis datasets, tables, listings, figures, and final reports to ensure accuracy and completeness
Support continuous improvement initiatives to enhance data processing efficiency and programming quality
Required Qualifications and Experience
Bachelor’s or Master’s degree in Computer Science, Statistics, Data Science, Life Sciences, or a related discipline
Minimum 2–5 years of programming experience, preferably within a clinical research, CRO, pharmaceutical, or biotechnology environment
Hands-on proficiency in SAS, R, Python, and/or Medidata Rave with Custom Functions
Strong understanding of clinical trial data structures, statistical analysis concepts, and data standards
High attention to detail with a strong commitment to data accuracy and quality
Excellent communication skills with the ability to collaborate effectively across global, cross-functional teams
What ICON Offers
Competitive compensation aligned with industry benchmarks
Flexible hybrid work model supporting work-life balance
Comprehensive health insurance and wellness programs
Retirement and long-term financial planning benefits
Global Employee Assistance Programme (TELUS Health) with 24/7 access to professional support
Life insurance and country-specific optional benefits
Continuous learning, upskilling, and global career advancement opportunities
Diversity, Equity, and Inclusion
ICON is committed to creating an inclusive and accessible workplace. All qualified applicants will receive equal consideration without regard to race, religion, gender, sexual orientation, gender identity, national origin, disability, or veteran status. Reasonable accommodations are available throughout the recruitment process.
Apply with Confidence
Candidates who may not meet every listed requirement are encouraged to apply. ICON values transferable skills, growth potential, and diverse experiences and considers applicants for this and future roles.
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