Study állás innen: Budapesti Megye

2026. 05. 03. | Teljes munkaidõ | Budapest | EUROAPIAnd Sponsors, focusing on simplification, harmonization, and cost optimization. The role involves working on projects and managing topics, ensuring continuity and flexibility in applications. Main responsibilities Acts as a counsellor/advisor throughout the entire life cycle (study, plan, design, build, run

2026. 05. 02. | Teljes munkaidõ | Budapest | IQVIAPurpose The Investigator Payments Analyst is accountable for budget planning, analytics and payment execution in a direct country or extended country group (OPC and satellite countries) in close collaboration with the SSO Study Start-Up Managers, SSO Clinical Project Managers and SSO Contracting

2026. 05. 02. | Teljes munkaidõ | Budapest | IQVIAFeedback in compliance with IQVIA SOP, ICH/ GCP guidelines, protocol requirements and regulatory compliance. Review of the Study Central Monitoring Plan Essential Functions Provide support to CMS leads on clinical deliverables on assigned projects as per the protocol, SOPs, respective regulation/guidelines

2026. 04. 30. | 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

2026. 04. 30. | 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. 30. | Teljes munkaidõ | Budapest | ZF GroupTechnical consulting to our internal HR stakeholders. Your profile as Application Consultant (m/f/d) SAP HR Payroll Degree in Mathematics, Computer Science, Business Informatics, or a comparable field of study - alternatively, a relevant vocational qualification with professional experience. Solid

2026. 04. 30. | Teljes munkaidõ | Budapesti | ClarioManagement deliverables for assigned studies, ensuring timelines and quality standards are met. Support study setup activities, including eCRF/TF design, database structure, and specifications, obtaining and providing necessary approvals. Understand study implementation and data collection requirements

2026. 04. 30. | 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