Study állás innen: Magyarország

2026. 02. 25. | Teljes munkaidõ | Budapest | ICONAssist in the planning, execution, and monitoring of clinical trials, ensuring adherence to protocol requirements, regulatory guidelines, and industry standards. - Coordinate study activities including site initiation, patient recruitment, data collection, and monitoring visits to ensure timely

2026. 02. 25. | Teljes munkaidõ | Budapest | IQVIADelivery. By assisting in the coordination and administration of the study activities from the start up to execution and close out, and within the Local Study Team (LST) the Clinical Trial Assistant ensures quality and consistency of study deliverables to time, cost and quality objectives. Essential

2026. 02. 25. | Teljes munkaidõ | Veszprém | Charles RiverInternational standards, Standard Operating Procedures (SOPs) and study plans and their amendments. • Maintain written and signed records of all audits and inspections as required and may sign records documenting the performance of audits and inspections and reporting to management. • Participate

2026. 02. 24. | Teljes munkaidõ | Budapest | IQVIADecisions during clinical study planning, execution, analysis, and reporting. This includes CRA/investigative site support as well as advanced safety and data analytics. Essential Functions Respond to protocol questions/CRAs/Sites under direction and supervision of the global study TMA. Collaborate

2026. 02. 24. | Teljes munkaidõ | ICONWill be doing - Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. - Ensuring protocol compliance, data integrity, and patient safety throughout the trial process. - Collaborating with investigators and site staff to facilitate smooth study conduct. - Performing

2026. 02. 24. | Teljes munkaidõ | ICONWhat you will be doing - Building and maintaining strong relationships with key stakeholders at clinical trial sites, including principal investigators, site coordinators, and research staff. - Providing support and guidance to site staff on study protocols, procedures, and regulatory requirements