2026. 01. 23. | Teljes munkaidõ | Budapest | IQVIAClinical Trial Educators (CTEs) collaborate with research staff and other stakeholders to drive trial recruitment and support study-specific training needs. The CTE acts as a strategic partner to both external and internal stakeholders to optimize the site experience and performance. They lead
Nézze később2026. 01. 21. | Teljes munkaidõ | Budapest | ExcelyaExpertise required for the successful completion of Excelya’s projects. Your Mission - Produce high‑quality scientific content in clinical medical writing (including clinical protocols, informed consent forms, clinical study reports, lay summaries), regulatory medical writing (CTDs 2.4-2.7) and medical
Nézze később2026. 01. 20. | Teljes munkaidõ | Budapest | 4flowOr more of experience in designing and managing complex cloud environments Bachelor's or Master's degree in Computer Science, Software Engineering, Information Technology or a related technical field of study Strong knowledge of AWS, Azure, GCP and multi-cloud strategies including a deep understanding
Nézze később2026. 01. 20. | Diákmunkák, Teljes munkaidõ | Budapest | 4flowOf our company with your personality, skills, knowledge, and experience You are pursuing a university degree in a STEM field, logistics, supply chain management, computer science, or a comparable field of study. An innovative mindset helps you dive deep and autonomously into new topics and technologies
Nézze később2026. 01. 20. | Teljes munkaidõ | Budapest | PSI CROJob Description PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners, while always focusing on patients' safety and well-being. Responsibilities - Serve as medical point of contact for internal project team, study sites and study sponsor
Nézze később2026. 01. 20. | Teljes munkaidõ | Budapest | PSIJob Description PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners, while always focusing on patients' safety and well-being. Responsibilities Serve as medical point of contact for internal project team, study sites and study sponsor
Nézze később2026. 01. 17. | Teljes munkaidõ | Budapest | PSIYou will Coordinate review and negotiation of clinical trial agreements and investigator grants between PSI staff and study sites. Perform administrative activities (documents collection/distribution, filing clinical trial agreements in the database and maintenance of local documentation). Customize
Nézze később2026. 01. 17. | Teljes munkaidõ | Budapest | PSIMatters Collaborate with internal departments in the preparation of clinical development plans, protocols, investigator brochures, annual reports, clinical study reports, manuscripts, and different scientific presentations Review and analysis of clinical data to ensure the safety of study participants
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