2026. 04. 17. | Teljes munkaidõ | Budapest | Bosch GroupUniversity professor), professional study or research (optional) Please choose category below which you would be interested in Mechatronics, Embedded system, IT, Artificial intelligence, Material science, Mechanical design, Measurement technology, Data management, SW design, SW testing, Signal processing
Nézze később2026. 04. 17. | Teljes munkaidõ | Budapest | AbbVieJob Description - Develop and maintain in-depth knowledge of the designated product (s) and therapeutic areas (TAs), including through participation in internal discussions, trainings, relevant congresses and seminars, and regular independent study of publications, literature and guidelines
Nézze később2026. 04. 16. | Teljes munkaidõ | Budapest | PSIstudy sites and study sponsor for medical matters related to the conduct of clinical trials per protocol and per GCP guidelines Advise clients, project teams, sites, regulatory agencies and third-party vendors on medical matters Collaborate with internal departments in the preparation of clinical
Nézze később2026. 04. 16. | Teljes munkaidõ | Budapest | ClarioResearch Associate I, you will join Clario’s Medical Imaging team in Hungary and help advance clinical trials through high-quality imaging data. In this role, you’ll coordinate site and operational activities from study start to close, ensuring timely delivery of service deliverables and supporting data
Nézze később2026. 04. 16. | Teljes munkaidõ | Budapesti | ClarioResearch Associate I, you will join Clario’s Medical Imaging team in Hungary and help advance clinical trials through high-quality imaging data. In this role, you’ll coordinate site and operational activities from study start to close, ensuring timely delivery of service deliverables and supporting data
Nézze később2026. 04. 16. | Teljes munkaidõ | Budapest | IQVIAFuntions Accountable to deliver Trial(s) on time, within budget, and with highest achievable quality. Assist in the review, development and/or writing of clinical trial documents and manuals, including but not limited to Protocol, Case Report Forms, informed consent forms, Clinical Study Report and other
Nézze később2026. 04. 16. | Teljes munkaidõ | Budapest | IQVIAIn this role, you 'll become an expert in Vendor Management for global clinical trials across all phases (Phase I-IV), ensuring seamless execution from study start-up through close-out. What We’re Looking For To excel in this role, you should bring Global Clinical Project Management experience Strong Vendor
Nézze később2026. 04. 16. | 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
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