Study állás innen: Magyarország

2026. 01. 20. | Teljes munkaidõ | Tatabánya | AptivWith clear instructions from Aptiv Plant or product engineering. Perform a risk assessment & feasibility study for reworks activities in sils & at Customer production lines. Coordinate Quality Improvements activities at customer & verify the effectiveness of solutions with solid breakpoints. Record, Report

2026. 01. 20. | Teljes munkaidõ | Budapest | ClarioMonthly balance sheet reconciliation book Assist with monthly close including analysis of P/L accounts Prepare monthly journal entries Support quarterly review and year-end audit requests QC study budget information against forecasting application Assist with preparation of monthly and quarterly reports

2026. 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

2026. 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

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

2026. 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

2026. 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

2026. 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