Clinical Research

• Partner with the global study leader to monitor study conduct and progress
• Identify, resolve, and escalate risks affecting study quality, timelines, and budget
• Support end-to-end operational study delivery from study setup through archival
• Set up and maintain internal systems, databases, tracking tools, and project plans
• Review clinical documents including protocols and informed consent forms
• Support development of monitoring, vendor management, protocol deviation management, and risk management plans
• Coordinate study-related activities and cross-functional team communications
• Prepare and schedule meetings
• Facilitate communications with regulatory teams, LOC, CROs, and third-party vendors
• Support country oversight, including recruitment, data completeness, compliance, local budgets, protocol deviations, and import license status
• Manage vendors and provide CRO oversight
• Oversee study-specific vendor deliverables
• Oversee delivery of clinical supplies, investigational products, and study materials
• Monitor eTMF completeness and inspection readiness, including setup, periodic reviews, missing-document follow-up, and safety report dissemination
• Manage change orders and expenses and ensure consistency between systems and agreements
• Escalate financial and operational issues to study stakeholders

Explore Trial Delivery Specialist – Clinical Trial Coordinator at Thermo Fisher Scientific. Review requirements and application details.

Trial Delivery Specialist – Clinical Trial Coordinator

Senior Clinical Data Manager – Data Standards

Senior Clinical Data Manager – Sponsor Dedicated

Remote Clinical Research jobs in Poland

Trial Delivery Specialist – Clinical Trial Coordinator

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