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The Sr. Reg Affairs Specialist supports a senior regulatory professional by executing against the global regulatory plan for one or more products.
We are currently seeking a Medical Information Manager. This individual will report to the Head of Medical Info within the Med Affairs Department.
Independently serve as clinical study statistician on multiple projects with limited supervision.
Designs, develops, evaluates and modifies SAS programs to analyze and evaluate clinical data.
Provide statistical/strategic inputs to the clinical development plans while supporting clinical trials within a program.