Clinical Assistant

• Provide support for critical day-to-day clinical study activities, including regulatory inspection readiness, in accordance with established protocols
• Collaborate with Clinical Operations/Study Manager, study teams, and CROs to support clinical study activities
• Perform departmental tasks as needed
• Review study documentation, including essential document packets, study plans, and informed consent forms
• Support and oversee risk-based monitoring
• Attend key team meetings and prepare minutes for selected studies
• Support regulatory inspection readiness, including SOP lists and storyboard collation
• Support clinical trial systems such as CTMS/TMF and associated activities
• Support vendor contract administration
• Support study close-out activities, including financial reconciliation
• Support additional ad-hoc activities as agreed with managers
• Collaborate with Legal, Insurance, R&D functions, CROs, and external vendors

Explore Clinical Study Assistant at ICON plc. Review requirements and application details.