2026. 03. 19. | Teljes munkaidõ | Budapest | IQVIASOPs and delivering targeted training. This role reports into Regulatory Affairs leadership and collaborates closely with study start-up, clinical monitoring, and project management colleagues to keep clinical trial regulatory filings on track and inspection‑ready. Key Responsibilities Serve
Nézze később2026. 03. 19. | Teljes munkaidõ | Budapest | Bosch GroupRelevant RF standards, specifications, protocols and regulations Qualifications - Successfully completed a degree in Electrical Engineering with a specialization in Radio Frequency Engineering or a comparable field of study. - Experience in the development of RF circuits, especially antennas. - Relevant
Nézze később2026. 03. 19. | Teljes munkaidõ | Budapest | Deutsche Telekom IT Solutions HUOr a comparable field of study or professional qualification. Expert knowledge and hands-on experience in IT architecture, cloud technologies (IaaS, PaaS, SaaS), and market-relevant cloud ecosystems. AI knowledge is a plus-help shape the future! Strong communication and presentation skills build confidence
Nézze később2026. 03. 18. | Teljes munkaidõ | Budapest | TechBiz Global GmbHResponsibilities - Perform statistical programming activities for clinical trials, including early-phase projects, indications, and publications - Lead at least one study team, providing technical and domain expertise - Manage and mentor a small team of 2-4 programmers (if required) - Develop and validate SAS
Nézze később2026. 03. 18. | Teljes munkaidõ | Budapest | TechBiz Global GmbHResponsibilities - Perform statistical programming activities for clinical trials, including early-phase projects, indications, and publications - Lead at least one study team, providing technical and domain expertise - Manage and mentor a small team of 2-4 programmers (if required) - Develop and validate SAS
Nézze később2026. 03. 18. | Teljes munkaidõ | Budapest | IQVIAEffective communication with project team through oral and written correspondence, status reports to ensure alignment with study timelines. Funtions Assists in the review, development and writing of clinical trial documents and manuals, including but not limited to study manuals, laboratory or biomarker
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