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The Centralized Monitor at IQVIA is responsible for managing the execution of assigned clinical studies from initiation through closeout. This role ensures that clinical study management and project deliverables are completed on time and in accordance with standard operating procedures (SOPs), policies, and practices. The position involves providing project-related support across multiple projects, sites, and teams, ensuring compliance with Good Clinical Practices (GCP) and regulatory requirements, and facilitating effective review processes to maintain subject safety and data integrity.