23.05.2024 | Full-time | F063 DB Global Technology SRLOf Information Security and with preference to prior experience in IS.Very strong ability to work focused and in a systematic way with only limited guidance and - in particular, under time pressure - exceptional attention to detailExcellent working experience of risk management, regulatory and senior stakeholder
Uita-te mai târziu23.05.2024 | Full-time | ING DeutschlandCompany restaurant Cooperation at eye level in a "you" culture, mobile working within the framework of operational, regulatory and legal requirements Strong networking
Uita-te mai târziu23.05.2024 | Full-time | Bytamic SolutionsMaximum value. Managing the product backlog you collect the requirements of all stakeholders for the product. These requirements are converted into tasks and sorted by priority. The Product Owner decides which tasks should be worked on next. Ensure that product features and roadmap align with regulatory
Uita-te mai târziu23.05.2024 | Full-time | PSIVisitsPerform CRF review, source document verification and query resolutionBe responsible for site communication and managementBe a point of contact for in-house support services and vendorsCommunicate with internal project teams regarding study progressParticipate in feasibility researchSupport regulatory team
Uita-te mai târziu23.05.2024 | Full-time | ProductLife GroupWe are seeking for a Regulatory Affairs Officer responsible for ensuring the delivery of regulatory activities performed onsite. Group 10 Responsibilities To contribute to the production of client administrative documents to be included in regulatory submissionsCompile regulatory dossiers
Uita-te mai târziu23.05.2024 | Full-time | F063 DB Global Technology SRLFor more critical cases, complaints or process nition, review and enhancement of Threat Detection & Response processes and toolsEnsuring that predefined processes and SLAs get rting of Information Security Incidents to Senior Management and orting the entire SOC team
Uita-te mai târziu23.05.2024 | Full-time | Worldwide Clinical TrialsEvery day to improve lives and we are looking for others who value this same pursuit. What you will do You will be a subject matter expert and local point of contact for activities supporting Regulatory submissions, site activation and maintenance for awarded projects. You will be responsible
Uita-te mai târziu23.05.2024 | Full-time | SanofiJob title Medical Lead ROOur Team Main responsibilitiesMedico-Regulatory, Health Economics & Market Access Provides product scientific expertise to Regulatory Affairs Department for registration support, labelling changes, or when requested by health authoritiesMedico-Marketing, Sales Force
Uita-te mai târziu23.05.2024 | Full-time | Dell Technology SrlWith the validation and risk assessment of models across all functions of DFS. A major focus of the role will be on the continued quality assurance of global credit application models and key European Banking & Finance regulatory models such as IFRS 9 ECL models and ICAAP models. The validation of these models
Uita-te mai târziu23.05.2024 | Full-time | EYSector. Each industry being different it faces different sets of risks, and you will have the opportunity to understand various businesses of the FSI clients, their accounting and regulatory requirements. Could your career journey be as unique as you are? What will you do? Stay curious, listen to client
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