About this role
The Statistical Programmer is a key team member responsible for creating and validating statistical programs for clinical trials, transforming raw data into analysis datasets, and supporting regulatory and data management teams. The role involves collaboration with internal and external stakeholders to ensure accurate and efficient data analysis and reporting to support medical device and pharmaceutical research. It offers an opportunity to work with advanced data standards and contribute to the development of innovative clinical trial solutions.
Required Skills
- SAS
- R Programming
- Clinical Data
- Data Standards
- Biostatistics
- Data Manipulation
- Analysis
- Programming
- Regulatory Compliance
- Database
About IQVIA
iqvia.comIQVIA is a leading global provider of data, technology, and advanced analytics focused on transforming healthcare and life sciences. The company empowers organizations to accelerate innovation, enhance patient outcomes, and expedite the market introduction of new treatments through comprehensive healthcare analytics and real-world evidence. With a commitment to Human Data Science, IQVIA combines its extensive expertise with innovative technology to improve health outcomes worldwide.
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