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Clinical Research Associate
JOB SCOPE:     Responsible for the implementation and coordination of clinical studies for IVD medical devices.  RESPONSIBILITIES:  Identify, evaluate, and establish clinical study sites. Conduct regular site monitoring visits (virtually and physically) and prepare reports for study initiation, monitoring, and close-out visits. Draft and/or provide input into Clinical Study Protocols, supporting plans and procedures, including Informed Consent Forms (ICFs), Monitoring Plans and Data Collection Forms in conjunction with the assigned Project Team. Assist with Institutional Review Board (IRB) submissions. Manage study budget and agreements with study sites. Manage study Trial


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