Regulator állás innen: Magyarország

2026. 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

2026. 03. 24. | Teljes munkaidõ | Budapest | IQVIARelevant sponsor or clinical research organization clinical site contracting experience Good negotiating and communication skills with ability to challenge. Strong legal, financial and/or technical writing skills. Strong understanding of regulated clinical trial environment and knowledge of drug

2026. 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

2026. 03. 24. | Teljes munkaidõ | Budapest | HirerooStrong exposure to the iGaming space, working with operators, suppliers and related entities, making it an ideal opportunity for someone looking to deepen their experience in a fast paced and regulated environment. Location Remote - Europe Responsibilities As a Lawyer, your broad responsibilities

2026. 03. 23. | Teljes munkaidõ | Budapest | Ceva Santé AnimaleIs seeking a Global Quality Systems Manager to lead and strengthen its Global Quality Systems . In this role, you will drive harmonization, standardization, and continuous improvement across the worldwide organization, ensuring CEVA’s Quality Management System is aligned with regulatory and market

2026. 03. 23. | Teljes munkaidõ | ICONIn a scientific or healthcare-related field. - Must have Prior experience in clinical research in CRO or Pharma company in admin position - KNwledge of clinical trial processes, regulations, and guidelines. - Excellent organizational and communication skills. - Ability to work collaboratively in a fast-paced

2026. 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

2026. 03. 23. | Teljes munkaidõ | Budapest | SanofiContribution of RS and affiliates and retrieve information from regulatory database and regional regulations. Participate in the maintenance and improvements of the current regulatory repositories already in place. Ensure with contributors the process compliance and timeliness. Enter associated data