Clinical Trial Associate

• Provide logistical support to one or more global study management teams through all phases of clinical study management
• Develop and maintain relationships with study management team members, affiliate teams, and vendors
• Assist the Clinical Trial Manager with communication between the study management team and affiliates
• Coordinate global study supplies using designated systems
• Coordinate and organize study-related meetings and develop presentation materials
• Consolidate study information for trackers and databases
• Support protocol feasibility, country, and site selection processes
• Support technical and logistical study processes
• Track and maintain study information and documentation and report study progress
• Maintain study management data, team contact details, country contacts, and distribution lists
• Track Health Authority, IRB, and IEC submissions and approvals in CTMS; identify delays and escalate issues
• Provide submission and supplementary documentation to affiliates or Product Development Regulatory
• Maintain completeness of the study-level Trial Master File under CTM direction
• Identify and contribute to best practices and process improvements
• Incorporate learnings and recommendations from study debriefs and best practices

Clinical Trial Associate jobs in Poland

Senior Clinical Trial Associate