Job Description
Position Summary
The Statistical Programmer II is responsible for developing and maintaining statistical programs to support clinical trial analysis and reporting. The role involves working closely with statisticians and clinical teams to generate analysis datasets, tables, listings, and figures while ensuring high data quality and regulatory compliance.
The position also focuses on managing complex datasets, supporting multiple clinical studies, and contributing to efficient statistical programming processes within clinical development projects.
Key Responsibilities
Develop and maintain statistical programs using R and SAS to support clinical trial analysis
Create and validate analysis datasets, tables, listings, and graphical outputs for clinical studies
Work with complex clinical datasets by sourcing, organizing, and interpreting data for statistical analysis
Develop codes and scripts to automate data processing and improve efficiency in statistical programming workflows
Utilize data visualization tools such as TIBCO Spotfire to create dashboards, calculated columns, and data filters
Collaborate with statisticians, data managers, and cross-functional clinical teams to support study deliverables
Evaluate existing programming processes and recommend improvements to increase productivity and accuracy
Support multiple clinical studies simultaneously and contribute to project or study-level programming activities
Provide guidance or support to junior programmers when required
Ensure compliance with clinical research standards and regulatory requirements across programming activities
Professional Experience Requirements
Minimum 3 years of experience in advanced SAS and R programming within clinical research or pharmaceutical environments
Experience with SQL and data management techniques for handling clinical datasets
Hands-on experience with TIBCO Spotfire or equivalent visualization tools
Understanding of the clinical trial lifecycle and drug development process from Phase I to Phase IV
Experience working with clinical data management systems and supporting statistical analysis workflows
Strong written and verbal communication skills
Apply Details
Apply via the company career portal for
Syneos Health
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Madrid |Cebu Province :
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Zagreb |Estonia :
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