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2 days ago
We are seeking a skilled Senior Statistical Programmer to join our team. The ideal candidate will have experience in all areas of statistical programming and be able to provide programming support for clinical trials.
The Senior Statistical Programmer will be responsible for providing technical expertise and guidance to the project team on statistical analysis, data management, and reporting.
Responsibilities:
- Provide statistical programming support for clinical trials
- Develop and maintain SAS programs for data manipulation and analysis
- Implement CDISC and other regulatory standards
- Follow internal SAS programming conventions
- Serve as programming lead on assigned studies
To be successful in this role, you will need:
- A 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.)
- Excellent oral and written communication skills, organizational skills, and attention to detail
We offer a competitive salary and benefits package, including:
- Opportunities for professional growth and development
- A collaborative and dynamic work environment
- Recognition and rewards for outstanding performance
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