Job Abstract

Responsible for the design, delivery and interpretation of clinical studies from first-in human through Ph 2 b, ensuring compliance with GCP and ethical / scientific integrity of studies. Lead ongoing monitoring of clinical data to ensure quality and safety, including SAE/ SUSAR/protocol deviations and periodic review of emerging safety data by SRC/ DM - Cs, and oversee the support of investigational sites on protocol related matters and investigation of unexpected trends in data. Lead clinical ... more details

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