2026. 01. 19. | Teljes munkaidõ | Budapest | ClarioBudget requirements, initiate purchase orders, review and approve invoices, and update study budget files. Monitor and report on expenses related to consultant use for live training; prepare and deliver requested reports and KPIs. Oversee invoicing for client training deliverables and manage software
Nézze később2026. 01. 17. | Teljes munkaidõ | Budapest | PSIExpectations, and best practices in clinical trial data management Collaborating cross-functionally to identify study-level challenges and deliver tailored data-driven solutions Qualifications Must have Degree in Data Science, Mathematics, Statistics, Computer Science or equivalent Minimum 4 years of R and R
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
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 | BYD EuropeAnd technical associations to stay informed of the latest industry trends and development requirements. Monitor updates to European road safety regulations and standards, study advancements in active safety technologies, and provide strategic input for innovative product design. - Competitive Benchmarking
Nézze később2026. 01. 17. | Teljes munkaidõ | Budapesti | ClarioAnd prevent issues from recurring through utilization of risk based and control concepts Data, processes, and systems implemented by Clario are compliant with applicable regulations, guidelines, and internal procedures through quality reviews of primary study documentation and software applications Manages
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