Study állás innen: Magyarország

2025. 06. 28. | 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

2025. 06. 28. | Teljes munkaidõ | Budapest | MOL MagyarországAnd students and assisting with archiving at the end of the process. - Supporting the onboarding and offboarding processes for dual and trainee students. - Managing study contracts, status management. - Preparing ad-hoc reports. EXPCTATIONS - University degree - Minimum 1 year of administrative experience

2025. 06. 28. | Gyakornoki állás, Teljes munkaidõ | Budapest | Hermes Schleifmittel GmbHAnd work on optimizations - we value new perspectives! What you need to bring with you - You are studying business administration, economics, industrial engineering or a similar field of study - You are confident in using Microsoft 365 tools such as Excel, PowerPoint and Teams (initial experience with SAP

2025. 06. 28. | Teljes munkaidõ | Budapesti | ClarioServices while promoting excellent customer service. You will lead the Planning and Setup, Monitoring, and Closeout phases of study management which includes Gathering customer requirements and relaying to internal teams Developing study documentation Distributing/tracking equipment Creating/distributing

2025. 06. 28. | Gyakornoki állás, Részmunkaidõ, Teljes munkaidõ | Budapest | Morgan StanleyFinancial markets and relevant industries Prepare portfolio stress testing analysis of credit risk exposures on lending and derivatives products Participate in innovative projects related to data analysis, visualization, and process automation You have Financial Risk and Capital if you are studying

2025. 06. 28. | Teljes munkaidõ | Budapest | Precision Medicine GroupPosition Summary The Senior Clinical Data Manager/Principal Clinical Data Manager is responsible and manages all aspects of the clinical trial data management process from study start up to post database lock for assigned projects. Standard Operating Procedures - Work Instructions (SOPs/WIs

2025. 06. 27. | Teljes munkaidõ | Budapest | IQVIAJob Overview Manage the execution of the assigned clinical study (ies) from initiation through to closeout. Ensure that clinical study management and project deliverables are on time and is in accordance with standard operating procedures (SOPs), policies and practices. To provide project related

2025. 06. 27. | Teljes munkaidõ | Budapest | IQVIAFor SAS programs used to access, extract, transform, review, analyze and submit clinical data for all requested analyses. Main Responsibilities and Accountabilities Collaborates with the study teams to design data structure and specifications for ad hoc and study deliverables including, but not limited