2026. 03. 07. | Teljes munkaidõ | Budapest | ClarioMatter expertise within client facing meetings as required Create and maintain specifications for study-specific implementations of Clario products and services Ensure consistency between trial data capture, data delivery and database structures Collaborate with Clinical Systems Translation & Licensing
Nézze később2026. 03. 07. | Gyakornoki állás, Teljes munkaidõ | Budapest | Morgan StanleyIn English, both verbal and written Interest to study identification of operational risk, measuring potential losses, managing risk, method of capital modelling, natural language
Nézze később2026. 03. 07. | Teljes munkaidõ, Tréning | Budapest | Bosch GroupDocumentation of results - Basic programming skills - Python knowledge Additional qualifications - Active university study status in Hungary for at least one more year - English language - Weekly minimum 20 hours Additional Information Get to know our #LikeABosch benefits We would like to help you GROW, so we
Nézze később2026. 03. 07. | Teljes munkaidõ | Budapesti | ClarioConduct needs analyses, develop high‑level and detailed designs, and create training content from concept through final production and rollout. Partner with internal teams and clients to gather training requirements and ensure content aligns with study, product, and protocol objectives. Produce raw
Nézze később2026. 03. 06. | Teljes munkaidõ | Budapest | IQVIANotifications. Essential Functions • Assist in study specific submissions document management and document collation for submission • Perform document quality and completeness checks • Transfer submission package to CTIS, make submission in CTIS and perform submission archiving. • Ensure the current submission
Nézze később2026. 03. 06. | Teljes munkaidõ | Budapest | IQVIAAnd facilitate efficient study start-up and maintenance. Create and review scientific, technical, and administrative documentation required for study initiation. Assess the contracting landscape and contribute to the analysis and dissemination of contracting intelligence across the company. Ensure contracting
Nézze később2026. 03. 05. | 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
Nézze később2026. 03. 05. | Teljes munkaidõ | Budapest | ICONStandards. You will work closely with Clinical Research Associates (CRAs), site staff, and cross-functional teams to help drive study start-up, maintenance, and close-out activities. What You Will Be Doing - Supporting site activation activities, including the collection, review, and tracking of essential
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