Conduct site monitoring responsibilities for clinical trials
Provide oversight, leadership, and guidance in the management and execution of clinical trials
Ensure protocol compliance and address site questions
Assist with study recruitment and site training
Manage study budget and act as referent for the sponsor
Perform various site visits and prepare accurate monitoring visit reports
Maintain regular contact with study sites for compliance and patient accrual
Participate in internal and client meetings as required

Graduation in a scientific health field EU
Certified Monitor in compliance with Italian CRO decree dated 15Nov2011
Ability to establish and maintain positive relationships with Sponsor, Site and Project Team members
Ability to autonomously manage monitoring activities

Clinical Research Associate, CRA

Key skills