Study állás innen: Budapesti Kerület

2026. 04. 24. | Teljes munkaidõ | Budapest | ICONstudy conduct. - Performing data review and resolution of queries to maintain high-quality clinical data. - Contributing to the preparation and review of study documentation, including protocols and clinical study reports Your Profile You will bring relevant clinical trial monitoring experience, along

2026. 04. 24. | Teljes munkaidõ | Budapest | ICONMonitoring patient safety and addressing any clinical issues that arise during the course of trials. - Collaborating with biostatisticians and data managers to analyze study data and provide clinical insights. - Engaging with investigators and site staff to facilitate effective trial management

2026. 04. 24. | Teljes munkaidõ | Budapest | ICONThe Nordic region (Sweden, Norway, Denmark, and Finland). As a Site Specialist I at ICON, you will be at the heart of study start-up, ensuring essential documentation and site activation activities are delivered efficiently, compliantly, and with a strong sense of partnership. Your work will directly

2026. 04. 23. | Teljes munkaidõ | Budapest | PSITo the area of expertise to site team members involved in patient recruitment Identify, track, and report patient enrollment progress throughout the study Analyze the protocol in order to provide the site with the support needed to improve the patient pathway Provide support to the project teams to ensure

2026. 04. 23. | Teljes munkaidõ | Budapest | PSI CROTo the area of expertise to site team members involved in patient recruitment - Identify, track, and report patient enrollment progress throughout the study - Analyze the protocol in order to provide the site with the support needed to improve the patient pathway - Provide support to the project teams

2026. 04. 22. | Teljes munkaidõ | Budapest | HITACHI ENERGY ITALY S.P.A.Postgraduate study/courses in economics and commercial management would be of advantage About 5 Years of experience working in HVDC and/or similar Business Substantial experience and knowledge of multidiscipline scopes of work Strong communication and interpersonal skills, with the ability to collaborate

2026. 04. 22. | Teljes munkaidõ | Budapest | IQVIAStep into a role where strategy meets impact. As a Clinical Supply Chain Manager, you will shape and drive the end‑to‑end supply strategy for new clinical trials. Using your ability to translate complex study protocols into smart kit designs and robust supply plans, you’ll ensure that every element

2026. 04. 21. | Teljes munkaidõ | Budapest | Nucs AIPrograms function to support our expanding portfolio of clinical collaborations, validation studies, and regulatory evidence generation. This is a new role designed to own the operational execution of our medical programs-from clinical study coordination and site management to data collection, protocol