Study állás innen: Magyarország

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. 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. 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 | ClarioBy patients and researchers worldwide. This position is part of a collaborative cross‑functional team responsible for customizing and configuring our platform to meet study‑specific requirements-directly contributing to how critical clinical data is collected, managed, and delivered. What We Offer Competitive

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

2026. 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

2026. 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