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. 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

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. 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 | 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. 14. | Teljes munkaidõ | Budapest | Nucs AIPrograms function to support our expanding portfolio of clinical collaborations, validation studies, and regulatory evidence generation. This is a new role designed to own the operational execution of our medical programs-from clinical study coordination and site management to data collection, protocol

2026. 03. 14. | Teljes munkaidõ | Budapest | Nucs AIMedical community. Working alongside the Medical Director and Associate Director of Medical Programs, you’ll translate clinical insights and study results into compelling scientific narratives, educational programs, and market-facing materials that build trust and drive adoption. You’ll also manage