Principal Clinical Database Engineer (FSP)

Skills:Proficiency in at least one programming environment (e.g., SAS, CDMS, EDC, SQL, VB, Java). Experience working with at least one system used within the Clinical Trial process (e.g. SAS, CDMS, EDC (Inform, RAVE, DataLabs), CTMS, Medical Safety Reporting). Relevant Clinical Trial industry experience. Knowledge of SOPs/Guidelines/Work Instructions/System Life Cycle methodologies, ICHGCP and any other applicable local and international regulations such as 21 CFR Part 11 and proven practical application. Team and Project leadership experience required.

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