• Ensure successful delivery of assigned clinical trial projects by aligning study specifications and deliverables with client, protocol, and internal requirements. • Clearly document and manage project scope, timelines, and expectations. • Coordinate cross‑functional activities including logistics, specimen management, data management, and laboratory operations. • Direct timelines and resource needs with relevant internal departments. • Ensure all validation and quality control requirements are met and documented according to SOPs and obtain all necessary internal and client approvals. • Organize and lead client meetings and training sessions; maintain complete documentation of all training. • Provide day‑to‑day project management through internal and external coordination throughout the project lifecycle. • Troubleshoot issues related to specimens, result reporting, and site compliance; provide timely resolutions or escalation as needed. • Monitor project progress through regular team meetings and provide updates and metrics to management. • Proactively identify project risks and escalate issues following global escalation policies. • Maintain consistent, clear communication with clients and internal leadership on project status. • Manage manual invoicing processes to ensure accuracy and alignment. • Collaborate with Quality Assurance during audits, inspections, and other QA/QC activities; respond promptly to information requests. • Complete all tasks in compliance with SOPs and policies and maintain required training documentation. • Support process improvement initiatives, standardization efforts, and SOP development or review. • Perform additional duties as assigned by management.