Regional Clinical Reseach Associate

Regionally based CRAs needed for several openings in Southern California, Northern California, Midwest, Northeast, and Southeast.

Responsible for ensuring that the rights, well-being and safety of human subjects are protected, performing site visits from pre-study to close out to monitor and ensure study/protocol compliance according to GCPs/ICH, and other regulatory agency guidelines. Assures that the reported data are accurate, complete and verifiable from source documents. Maintains ongoing and continuous professional communication with the clinical site and the study team throughout the duration of the study. Implements Integrium and project specific monitoring expectations, to include: coordination of site visits within work scope-specific timelines.