Clinical Research Associate, Site Management - Italy

Clinical Research Associate, Site Management position to engage in structured training program to gain knowledge and skills required to independently conduct clinical monitoring visits.

Requirements

• Complete therapeutic, protocol and clinical research training
• Gain experience in study procedures by working with experienced clinical staff
• Perform site monitoring visits in accordance with contracted scope of work and good clinical practices
• Administer protocol and related study training to assigned sites
• Evaluate the quality and integrity of study site practices
• Manage the progress of assigned studies
• Ensure copies/originals site documents are available for filing in the Trial Master File (TMF)
• Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans
• Collaborate and liaise with study team members for project execution support

Benefits

• Generous Paid Time Off
• 401k Matching
• Retirement Plan
• Visa Sponsorship
• Four Day Work Week
• Generous Parental Leave
• Tuition Reimbursement
• Relocation Assistance