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Principal Statistical Programmer
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Full-time
- The Principal Statistical Programmer will lead and support all programming activities per the project strategies and should be able to work independently implementing and driving the programming to support ongoing clinical studies and requests for study report, regulatory submission, and ad hoc/post hoc analysis.
- Understand the scope of work, plan and complete the deliveries and timelines with the study team, programming lead and management
- Proficiency in SAS programming skills in a clinical data environment with excellent analytical skills.
- Knowledge of other programming languages such as R, Python etc.
- Good knowledge of pharmaceutical clinical development (i.e., understanding of statistical concepts, techniques, and clinical trial principles).
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