Clinical Research Associate (CRA)Clinical Research Associate (CRA)The Clinical Research Associate (CRA) will be responsible for the oversight and management of clinical trials, ensuring compliance with regulatory requirements and maintaining high standards of data quality and integrity. This role involves close collaboration with cross-functional teams, including project management, regulatory affairs, and clinical operations.Key responsibilities include:Monitoring clinical trial progress and ensuring adherence to study protocolsConducting site visits and audits to verify compliance with regulatory and company standardsManaging and coordinating study start-up activities, including site initiation visits and trainingOverseeing data collection, management, and reporting processesProviding training and support to site staff and study teamsEnsuring timely and accurate reporting of adverse events and study progressThe ideal candidate will possess a strong background in clinical research, with a deep understanding of regulatory requirements and a commitment to excellence in clinical trial management.
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