2026. 03. 24. | Teljes munkaidõ | Budapest | DeloitteCommunication skills• Highly motivated, “can do” attitudeAdvantages, if you have• Regulatory VAT, CIT compliance knowledge• Experience with SAP SD or MM Tax Determination• Participation in SAP rollout or implementation project• Tailoring DRC reports for multiple Central European countries• Work experience
Nézze később2026. 03. 24. | Teljes munkaidõ | Budapest | IQVIAOf application/documents for submissions to Regulatory Authority for the duration of the study, and in line with local regulations. Ensures timely preparation of country financial Study Management Agreement (fSMA) and maintains accurate study budget in Sponsor clinical studies financial system by regular checks
Nézze később2026. 03. 24. | Teljes munkaidõ | Budapest | DeloittePrevious internships or project experience related to AI and finance Knowledge of financial auditing procedures and regulatory requirements Background in working with structured and unstructured data, embeddings, vector databases, and data pipelines Understanding of responsible AI, data governance
Nézze később2026. 03. 24. | Teljes munkaidõ | Budapest | WiseWith regulatory obligations, and fostering a strong sense of community within the team. As an AML Investigations Team Lead, your primary duties include building and developing your team, optimizing operational processes, and collaborating with other teams to enhance efficiency and customer experience. Here’s how
Nézze később2026. 03. 23. | Teljes munkaidõ | Budapest | ICONChecks to ensure data integrity prior to analysis. - Participating in the creation of tables, listings, and figures (TLFs) and contributing to documentation for clinical study reports and regulatory submissions. - Gaining hands‑on experience with CDISC standards, with a particular focus on ADaM dataset
Nézze később2026. 03. 22. | Teljes munkaidõ | Budapest | ParexelTo work. We are unable to provide visa sponsorship or relocation support for this role. About the Role We're looking for an experienced Audit Specialist to lead Sponsor Audits and Regulatory Inspections across our European operations. You'll provide expert guidance to project teams, drive audit
Nézze később2026. 03. 21. | Teljes munkaidõ | Budapest | WerfenFeasibility against applicable regulations in targeted markets, under supervision Contributing to the preparation and maintenance of regulatory documentation (e.g. Design History Files, Technical Documentation) Supporting the maintenance of regulatory profiles for assigned IVD medical devices Assisting
Nézze később2026. 03. 20. | Teljes munkaidõ | Budapest | SogelinkDedicated to managing commercial public domain occupancy. It digitalizes permits, market rights, fee collection, and regulatory workflows within an MVC-based platform, with dedicated APIs supporting mobile and tablet clients. As part of our Ambition 2030, the platform is evolving towards a modern
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