2026. 03. 19. | Teljes munkaidõ | Budapest | ContinentalOf internal control systems and compliance with internal standards - policies and regulatory requirements. Compile audit report and present the results to the management Propose measures to address identified risks and provide actionable advice to the business. Advise management on the development
Nézze később2026. 03. 19. | 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. 19. | Teljes munkaidõ | Budapest | ContinentalOf internal control systems and compliance with internal standards - policies and regulatory requirements. - Compile audit report and present the results to the management - Propose measures to address identified risks and provide actionable advice to the business. - Advise management on the development
Nézze később2026. 03. 19. | Teljes munkaidõ | Budapest | EYProcesses, and design and implement systems to effectively manage these areas governed by regulatory bodies globally (FDA, EMA, etc.). Do you have consulting and Regulatory systems experience and a passion for helping customers optimize their RIM processes? As a RIM Consultant, you will be responsible
Nézze később2026. 03. 19. | Teljes munkaidõ | Budapest | CitiResponsibilities Work with stakeholders in Regulatory Reporting function of Finance to develop and deploy digital solutions that automate the creation of financial reports for internal use or for financial regulators. Design, Develop and Deploy automation solutions using low‑code technologies and rule engines
Nézze később2026. 03. 19. | Teljes munkaidõ | Budapest | Deutsche BankHome and abroad, securing their lasting success and financial security. Know Your Client (KYC) (f/m/x) is responsible for ensuring client onboarding and ongoing expectations are in line with regulatory standards and jurisdictions. Responsibilities Focuses on client onboarding (COB) and exceptions
Nézze később2026. 03. 19. | Teljes munkaidõ | Budapest | IQVIAAs an experienced individual contributor within IQVIA Biotech’s Regulatory Affairs team, you’ll operate under limited supervision to drive clinical trial regulatory strategy and delivery across complex, multi‑stakeholder projects. You’ll lead cross‑functional regulatory workstreams, prepare and review clinical
Nézze később2026. 03. 19. | Teljes munkaidõ | Budapest | MaerskEnsure the team is trained and operates in alignment with global Maersk standards and local regulatory requirements. Take full responsibility for the customer
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