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7 days ago
We are seeking a highly skilled statistical programmer with extensive experience in statistical programming, particularly in SAS, and a strong understanding of CDISC and other regulatory standards.
The ideal candidate will be responsible for providing programming support for clinical trials, including developing and validating statistical outputs, creating and maintaining project timelines, and supporting the development of tools and macros to improve quality and efficiency of processes.
Key Responsibilities- Provide programming support for clinical trials
- Develop and validate statistical outputs
- Create and maintain project timelines
- Support the development of tools and macros to improve quality and efficiency of processes
- Prepare programming specifications for SDTM, ADaM and other derived datasets
- Bachelor's degree in Statistics, Computer Science, or a closely related field
- Minimum of 4 years direct SAS programming experience in pharmaceutical development or CRO environment
- Good knowledge of medical terminology and conduct and analysis of clinical trials
- Knowledge of relevant industry data standards (e.g. CDISC SDTM, ADaM, etc.)
- A dynamic and inclusive work environment
- Opportunities for professional growth and development
- A competitive salary and benefits package
At our company, we value diversity and inclusion and are committed to creating an environment that is welcoming to all employees. We believe that a diverse staff allows us to effectively draw on different perspectives and enhance our efficiency and effectiveness.
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