internal progression opportunities. As a Clinical Research Associate (CRA) you will coordinate all aspects
Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions Perform site monitoring visits (selection, init
activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to delivery. Essential Functions Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU)
activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to delivery. Essential Functions - Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU)
protection training, preferably CRA (Clinical Research Associate) training. Skills Required: 1.Excellent
ensures what we do, we do well.As a Clinical Research Associate at ICON, you'll work within a large-scale
consisting of Clinical Trial Managers, Clinical Research Associates, Clinical Trials Associates, and consultants responsibilities of Clinical Trial Managers, Clinical Research Associates, and Clinical Trials Associates is required
compliance with targets Key Stakeholders: - Clinical Research Associates, Clinical Trial Administrators, Clinical
ensures what we do, we do well. As a Clinical Research Associate at ICON, you'll work within a large-scale
ensures what we do, we do well. As a Clinical Research Associate at ICON, you'll work within a large-scale