A regular day will see you:

• Review and implement clinical trial protocols and procedures, coordinating laboratory setup and testing requirements.
• Coordinate pathology requirements for clinical trials and research projects from setup through to delivery.
• Combine scientific expertise with strong administration, including trial documentation, data, samples and laboratory coordination.
• Supply accurate financial and data management, including costings, reporting and trial-related financial administration.
• Support researchers, trial coordinators and laboratory teams, responding to enquiries, resolving operational issues and maintaining effective communication throughout trial activities.
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