Senior Clinical Research Associate – Site Monitoring

A leading clinical research organization is seeking a CRA II to manage study sites and ensure compliance with protocols. Responsibilities include overseeing patient safety, conducting site visits, and preparing monitoring reports. The ideal candidate will have a minimum of two years of experience in clinical research, particularly in oncology trials. A 4-year degree in a life science or healthcare discipline is required.

This role involves significant overnight travel and offers a competitive salary package, including healthcare and a discretionary bonus.
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