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2026. 04. 26. | Teljes munkaidõ | Budapest | IQVIAJoin IQVIA as an Associate Clinical Supply Chain Manager, and you will support the end‑to‑end clinical supply chain strategy for new clinical trials. In this position, you’ll collaborate closely with internal teams and external partners, ensuring on-time delivery of supplies (Investigational Medicin

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. 09. | Teljes munkaidõ | Budapest | ParexelRegulations and guidance, ensuring adherence to established processes, SOPs, and work instructions. Working within Parexel's consulting framework, you will provide regulatory leadership while delivering projects that meet both client and Parexel quality expectations. The role can be full remote or office

2026. 04. 04. | Teljes munkaidõ | ParexelWith the same active substance are globally aligned and leads the Global Labeling Committee assessment of proposed changes to the CCDS, including management of the exception process between the CCDS and the USPI and EU SmPC. The role can be home or office based in various European locations. Key

2026. 03. 31. | Teljes munkaidõ | Budapest | ParexelOf proposed changes to the dCCDS/CCDS, including management of the exception process between the CCDS and the USPI and EU SmPC. The role can be home or office based in various European locations. Key Responsibilities Generates and maintains the development Company Core Data Sheet (dCCDS), the Company Core

2026. 03. 26. | Teljes munkaidõ | Budapest | ParexelWith the same active substance are globally aligned and leads the Global Labeling Committee assessment of proposed changes to the CCDS, including management of the exception process between the CCDS and the USPI and EU SmPC. The role can be home or office based in various European locations. Key

2026. 03. 26. | Teljes munkaidõ | ParexelOf proposed changes to the dCCDS/CCDS, including management of the exception process between the CCDS and the USPI and EU SmPC. The role can be home or office based in various European locations. Key Responsibilities Generates and maintains the development Company Core Data Sheet (dCCDS), the Company Core

2026. 03. 22. | Teljes munkaidõ | ParexelLeaders. This is an opportunity to make a significant impact on global Regulatory Affairs projects while contributing to business growth and client success. The role can be home or office based in various European locations. Role Responsibilities Lead Client Solutions & Business Development Act