Study állás innen: Magyarország

2026. 04. 22. | Teljes munkaidõ | Budapest | IQVIAStep into a role where strategy meets impact. As a Clinical Supply Chain Manager, you will shape and drive the end‑to‑end supply strategy for new clinical trials. Using your ability to translate complex study protocols into smart kit designs and robust supply plans, you’ll ensure that every element

2026. 04. 21. | 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. 04. 21. | 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

2026. 04. 21. | 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. 04. 21. | 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. 04. 21. | Teljes munkaidõ | Budapest | IQVIAIn partnership with Business Development and may lead the presentation for smaller, less complex regional studies. • May be responsible for delivery and management of smaller, less complex, regional studies. • Develop integrated study management plans with the core project team. • Accountable for the execution

2026. 04. 21. | 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. 04. 21. | 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