2025. 12. 07. | Teljes munkaidõ | Budapest | DeloitteDescription & Requirements Who we are looking for university/college degree in appropriate field of study or relevant work experience but ideally IT with business interests or Economic sciences with IT interests 3 years of experience in analyzing and gathering business requirements in multinational
Nézze később2025. 12. 06. | Teljes munkaidõ | Budapest | IQVIAClinical Trial Educators (CTEs) collaborate with research staff and other stakeholders to drive trial recruitment and support study-specific training needs. The CTE acts as a strategic partner to both external and internal stakeholders to optimize the site experience and performance. They lead
Nézze később2025. 12. 04. | Teljes munkaidõ | Budapesti | ClarioAnd 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 (CSTL) to confirm correct versions of copyrighted questionnaires
Nézze később2025. 12. 04. | Teljes munkaidõ | Budapest | ClarioAnd 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 (CSTL) to confirm correct versions of copyrighted questionnaires
Nézze később2025. 12. 03. | Teljes munkaidõ | Budapest | Process SolutionsEnsure that personnel records are always accurate and up to date. This role is perfect for you if you… you’d like to learn the practical side of payroll, whether you’re a recent graduate or still studying, you are currently pursuing studies or already have a Social Security and Payroll Administrator
Nézze később2025. 12. 02. | Teljes munkaidõ | Budapest | ICONAnd therapies. What you will be doing - Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. - Ensuring protocol compliance, data integrity, and patient safety throughout the trial process. - Collaborating with investigators and site staff to facilitate smooth study
Nézze később2025. 11. 26. | Teljes munkaidõ | ParexelAnd works with minimal supervision to support various programming activities related to the analysis and reporting of clinical study data. In addition, the Statistical Programmer II may fill the Statistical Programming Lead role (or part of that role) on small, non-complex projects. What You'll Do
Nézze később2025. 11. 25. | Teljes munkaidõ | Budapest | IQVIAJob Overview Clinical Research Associate performs monitoring and site management work to ensure that sites are conducting the studies and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions • Perform site
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