
Senior Clinical Project Support Specialist provides operational support and coordination for global clinical trials, ensuring efficient execution from planning through close-out. Manages trial documentation, systems, communication, and logistics in compliance with SOPs, ICH-GCP, and regulatory requirements. Collaborates with global and regional stakeholders, vendors, and trial teams. Monitors trial progress, budgets, and system data, identifying risks and implementing corrective actions. Prepares project plans, status updates, reports, and presentation materials. Supports reporting, trial close-out activities, and preparation of key deliverables. Coordinates logistics for trial meetings, materials, and supplies. Contributes to quality oversight, inspection readiness, and best practices in clinical trial conduct. Acts as a key point of contact for trial-related systems, documentation, and operational queries.