
Data Science Specialist
4 days ago
Our organization seeks a highly skilled Senior Statistical Programmer to support clinical trials. This individual will provide programming expertise, ensuring accurate and high-quality statistical outputs.
- Serves as programming lead on assigned studies, coordinating activities with support programmers and ensuring accuracy and completeness.
- Develops project timelines, creates tools and macros to improve quality and efficiency of processes, and prepares programming specifications for SDTM, ADaM, and other derived datasets.
- Applies knowledge of SAS programming to program/develop and/or validate statistical outputs according to the statistical analysis plan and other specifications.
- Reviews and provides input on case report form design and serves as a mentor to other programmers.
Additional Responsibilities:
- Maintains awareness of scope of work to actual work, alerting management of potential change orders or resourcing needs.
- Works effectively with cross-functional team members to ensure accurate and high-quality statistical outputs.
- Promotes visibility outside of the functional area and effectively interacts cross-functionally and in industry.
Requirements:
- 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 are required.
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