Statistical Programmer II (Data Scientist)
Locations: Bangalore (India), Paris (France), Madrid (Spain), Swansea (UK), Warsaw (Poland) | Multiple Global Locations Available
Work Model: Office or Home (Hybrid/Remote)
Employment Type: Full-Time
Posted: 6 Days Ago
Job Requisition ID: JR138151
Company: ICON plc
About ICON plc
ICON plc is a global leader in healthcare intelligence and clinical research, partnering with pharmaceutical, biotechnology, and medical device organizations to accelerate the development of innovative therapies. ICON is committed to scientific rigor, regulatory excellence, and fostering an inclusive, high-performance work culture across its global operations.
Role Overview
ICON is hiring a Statistical Programmer II (Data Scientist) to support advanced statistical programming and data visualization activities for global clinical trials. This role is critical to the development, validation, and delivery of high-quality statistical outputs that enable accurate interpretation of clinical trial data and regulatory submissions.
The successful candidate will work closely with biostatistics, clinical data science, and cross-functional teams to implement robust programming solutions using modern statistical and data science technologies.
Key Responsibilities
Design, develop, and validate statistical programming solutions for clinical trial data analysis and reporting
Build and maintain R and R Shiny applications to support interactive data visualization and statistical reporting
Collaborate with biostatisticians and study teams to translate analysis plans into accurate programming deliverables
Prepare, review, and maintain statistical analysis plans (SAPs), programming specifications, and derived datasets
Ensure full compliance with ICH-GCP guidelines, regulatory standards, and internal SOPs
Perform quality control checks to ensure data integrity, traceability, and reproducibility
Mentor junior programmers and contribute to training initiatives and best-practice development
Required Qualifications and Experience
Bachelor’s degree in Statistics, Mathematics, Computer Science, Data Science, or a related discipline; Master’s degree preferred
Minimum 5 years of end-to-end statistical programming experience within the clinical research, CRO, pharmaceutical, or biotechnology industry
Strong proficiency in R and R Shiny; experience with SAS is highly preferred
Exposure to Python and modern data science frameworks is an advantage
Solid understanding of clinical trial data structures, statistical methodologies, and regulatory expectations
Demonstrated ability to manage complex datasets with strong attention to detail and analytical rigor
Excellent communication skills with the ability to explain statistical concepts to both technical and non-technical stakeholders
Ability to work independently while collaborating effectively within global, cross-functional teams
What ICON Offers
Competitive, market-aligned compensation
Flexible working model with office or home-based options
Comprehensive health and wellness benefits
Retirement and long-term financial planning programs
Global Employee Assistance Programme (TELUS Health) with 24/7 access to professional support services
Life insurance and employee well-being initiatives
Continuous learning and career advancement opportunities within a global CRO environment
Commitment to Diversity and Inclusion
ICON is dedicated to fostering an inclusive and accessible workplace. All qualified applicants will receive equal consideration regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status. Reasonable accommodations are available throughout the recruitment process.
Apply with Confidence
Candidates who do not meet every listed requirement are still encouraged to apply. ICON values potential, transferable skills, and diverse experience and will consider applicants for this and future opportunities.
Gujarat :
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