Study állás innen: Magyarország

2026. 03. 24. | Teljes munkaidõ | Budapest | PurolabsBriefs, and work with editors and creators to produce ads that convert at scale. This is a performance role. Data guides everything. You'll live inside our ad accounts, study what's working, and use those insights to develop the next round of winning creatives. Creative instinct matters, but the numbers

2026. 03. 24. | Teljes munkaidõ | Budapest | IQVIAAnd countries as applicable to the position, to successfully deliver the agreed project scope in compliance with sponsor requirements and/or the RSU Management Plan. Provide specialist legal, operational and financial contracting support to the Study Teams, as applicable to site agreements to facilitate

2026. 03. 24. | Teljes munkaidõ | Budapest | IQVIAGlobal Trial Delivery Manager services provide for the global coordination of clinical trial management activities for internally managed and/or outsourced trials. These services lead the Study Management Team (SMT) and ensure global clinical operations deliverables progress according to agreed

2026. 03. 23. | Teljes munkaidõ | Budapest | IQVIAWill be working with the client directly to manage deliveries. The CMA contributes to the execution of the Centralized Monitoring process by performing the setup, programming and refresh(es) of the Centralized Monitoring platform, according to the study-specific Centralized Monitoring Plan (CMP). Main

2026. 03. 23. | Teljes munkaidõ | ICONWhat you will be doing - Assist in the coordination and administration of clinical trials, ensuring compliance with protocols and regulatory requirements. - Maintain and organize clinical trial documentation, including study files, essential documents, and regulatory submissions. - Support

2026. 03. 22. | Teljes munkaidõ | Budapest | IQVIAPerforms review of the Clinical Study Report (CSR) and patient narratives. Attends Kick-Off meetings, weekly team meetings, and client meetings, as needed or requested. Available 24/7 to respond urgent protocol -related questions from investigative sites, in accordance with local labor laws. May require

2026. 03. 19. | Teljes munkaidõ | Budapest | ClarioAnd communicate the Data Management Plan (DMP) in collaboration with Sponsors and internal Clinical Data Management teams Determine and document standard and study‑specific edit checks and data processing guidelines to ensure clean, high‑quality data Collaborate with internal teams on study setup requirements

2026. 03. 19. | Teljes munkaidõ | Budapesti | ClarioAnd communicate the Data Management Plan (DMP) in collaboration with Sponsors and internal Clinical Data Management teams Determine and document standard and study‑specific edit checks and data processing guidelines to ensure clean, high‑quality data Collaborate with internal teams on study setup requirements