R&G US Inc. is a leading Contract Research Organization (CRO) providing full services for clinical trial and entire drug life cycle. Led by former FDA experts and industry experts, R&G US can provide end-to-end services in strategic planning, clinical trial design, statistical analysis, SAS programming, data management, medical writing, medical monitoring, pharmacovigilance, and Data Monitoring Committee services. R&G US had extensive experience to support submissions to FDA, EMA, PMDA and NMPA. R&G US's goal is to provide the best service to the clients and work as one team to lower costs, shorten development time, and increase the success probability of products. You may find more information at .
If you are interested, please email your CV to: info@rgpharmaus.com.
As a biostatistical/SAS programmer I, you are responsible for the following tasks:
Minimum Requirements:
Citizenship:
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