06.06.2024 | Full-time | Broadway GamingExperience and satisfaction. Keeping our customers’ information up to date, in line with regulatory and legislative requirements. Collaborating with multiple disciplines within the company to achieve resolutions both industry-related and on a customer level. Conducting competitor research. Working within our
Uita-te mai târziu06.06.2024 | Full-time | PharmiwebDescription Site Start-Up Regulatory Coordinator with Portuguese AND/OR Italian - single sponsor (FSP)/Site Contracts support Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs
Uita-te mai târziu06.06.2024 | Full-time | PharmiwebFor clinical studies across various phases, ensuring adherence to applicable regulations and principles of ICH-GCP. Responsibilities Travel to sites to carry out site selection, initiation, monitoring and close-outs. Support the development of a subject recruitment plan. Evaluate the quality and integrity
Uita-te mai târziu06.06.2024 | Full-time | PharmiwebParexel is in the business of improving the world’s health. We do this by providing a suite of biopharmaceutical services that help clients across the globe transform scientific discoveries into new treatments. From clinical trials to regulatory, consulting, and market access, our therapeutic
Uita-te mai târziu06.06.2024 | Full-time | Siemens EnergyOf security -level Knowledge and understanding of the power generation industry and domain in which the software product liarity with regulatory compliance requirements relevant to data management and software work and adaptability Demonstrated ability
Uita-te mai târziu06.06.2024 | Full-time | PharmiwebIn Romania . Responsibilities include All details of site management as prescribed in the project plans Recruitment of potential investigators, preparation of EC submissions, notifications to regulatory authorities, translation of study-related documentation, organization of meetings and other tasks
Uita-te mai târziu06.06.2024 | Full-time | ProclinicalFor clinical studies in phases I - IV, ensuring adherence to applicable regulations and principles of ICH-GCP. Responsibilities will includeConduct a variety of different site visits. This is inclusive of selection, initiation, monitoring and close-out visitsSupporting the development of a subject recruitment
Uita-te mai târziu06.06.2024 | Full-time | IT Human ResourcesImplementations. Strong understanding of local financial regulations and reporting requirements. Ability to communicate effectively with local banks and regulatory bodies. Experience with VAT, Intrastat, and automated invoicing systems. Excellent problem-solving skills and attention to detail. Flexibility
Uita-te mai târziu06.06.2024 | Full-time | ADPOnsibilities He/she is the client's privileged contact in the implementation process, working closely with Celergo's global partners to help the client analyse and implement payroll regulations in accordance with legislation and guarantee the highest level of orm analysis activities for defining
Uita-te mai târziu06.06.2024 | Full-time | DeloitteInvolving regulated entities in the financial sector (due diligence; drafting and negotiation of transaction documents;inter-bank mergers (including cross-border mergers); transfer of business projects etc.), including throughout the authorization proceedings in front of the regulator (, acquisition
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