Senior Clinical Data Science Programmer
Location: Chennai, Bangalore, India
Work Model: Office with Flex (Hybrid)
Employment Type: Full-Time
Posted: 6 Days Ago
Job Requisition ID: JR140436
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 committed to scientific excellence, data integrity, regulatory compliance, and building an inclusive, high-performing workforce.
Position Summary
ICON is seeking a Senior Clinical Data Science Programmer to support the development, validation, and execution of advanced programming solutions for clinical trial data analysis and reporting. This role plays a critical part in ensuring accurate data transformation, high-quality statistical outputs, and regulatory-ready deliverables across global clinical studies.
The successful candidate will work closely with clinical data scientists, biostatisticians, and cross-functional stakeholders to deliver efficient, compliant, and scalable programming solutions that support clinical development programs.
Key Responsibilities
Develop, validate, and maintain clinical data science programming solutions for data analysis and reporting
Generate and review statistical datasets, tables, listings, and figures (TLFs) in support of clinical study reports and regulatory submissions
Collaborate with biostatistics and clinical data science teams to align programming outputs with study objectives and analysis plans
Apply and promote programming best practices, coding standards, and quality control processes
Ensure data accuracy, traceability, and compliance with industry regulations and internal SOPs
Identify opportunities to enhance efficiency through automation and emerging data science tools
Stay current with advancements in programming languages, clinical data standards, and data management technologies
Required Qualifications and Experience
Bachelor’s or Master’s degree in Computer Science, Statistics, Data Science, Life Sciences, or a related discipline
5–8 years of hands-on experience in clinical data programming within a CRO, pharmaceutical, or biotechnology environment
Strong proficiency in SAS and/or R; exposure to Python is an advantage
Solid understanding of clinical trial data structures and workflows, including regulatory deliverables
Proven ability to work independently while collaborating effectively in cross-functional, global teams
Strong analytical, problem-solving, and organizational skills with high attention to detail
Excellent written and verbal communication skills
What ICON Offers
Competitive salary aligned with global industry benchmarks
Hybrid and flexible working model
Comprehensive health insurance coverage
Retirement and long-term financial planning benefits
Global Employee Assistance Program (TELUS Health) with 24/7 professional support
Life insurance and wellness programs
Career development opportunities within a global CRO environment
Diversity and Inclusion
ICON is committed to creating an inclusive and accessible workplace. All qualified applicants will be considered without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status. Reasonable accommodations are available throughout the hiring process.
Apply with Confidence
If you are passionate about clinical data science and may not meet every requirement listed, ICON encourages you to apply. Your skills and experience may be a strong fit for this or other opportunities within the organization.
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