Duties include working on protocols, statistical analysis plans (SAPs), CRF design, and study initiations; performing statistical analyses, validating analysis datasets and validating results from studies and pooled datasets in diabetes area.
Provide statistical support for the Diabetes area. Work to be completed will focus on:
supporting statistical activities for Phase III program from study design, protocol development, SAP development, study initiation, validating analysis datasets and TLGs
Experience in supporting trials in diabetes area is a plus, but not necessary. Should have very good writing, communication and programming skills, especially SAS. Good knowledge in R is a plus, but not necessary
Biostatistician with at least 2 years of experience supporting Phase 2/3 trials.
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