Clinical Trial Assistant

• Support the operational management of international clinical studies
• Work closely with Clinical Project Managers and CRA teams across multiple countries
• Manage Sponsor Trial Master Files (eTMF) and essential study documentation
• Support preparation, maintenance, and tracking of Investigator Site Files (ISF)
• Contribute to study feasibility activities and site selection processes
• Support submissions to regulatory authorities and ethics committees
• Assist with study start-up and site activation activities
• Provide operational support to Clinical Project Managers and Clinical Research Associates (CRAs)
• Organize study meetings, prepare agendas, participate in discussions, and draft meeting minutes
• Ensure clinical documentation is complete, accurate, and compliant with ICH-GCP requirements
• Collaborate with cross-functional teams across international clinical studies
• Provide back-up support for other clinical operations team members when required

Explore Clinical Trial Assistant at Excelya. Review requirements and application details.