06.06.2024 | 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 | Société Générale AssurancesResponsibilities· Participate in the design and implementation of the methodologies used in the management of the market & liquidity risks (identification, valuation, control, reporting); perform their regular updates, in line with internal or regulatory evolutions· Perform the daily capture, monitoring, control
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 | 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
Uita-te mai târziu06.06.2024 | Full-time | Craiova | 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 | IQVIAAssociate Site Manager with FrenchReal-World EvidenceHybrid EMEAJoin us on our exciting journey!IQVIA Real-World Evidence (RWE) teams work with clients to help them collect and use real-world data to generate evidence to meet the needs of regulators, payers, providers, and approach
Uita-te mai târziu06.06.2024 | Full-time | IQVIAAnd ntial FunctionsInterpret clinical trial protocols to create and execute an effective clinical trial supply chain solutionCreate master English label text in accordance with relevant regulatory frameworkCreate and maintain demand forecasts and packaging plans so that packed clinical supplies are readily
Uita-te mai târziu06.06.2024 | Full-time | F063 DB Global Technology SRLDescription ITAO will be responsible to ensure the applications that he/she owns is fully compliant to DB policies and standards and adheres to regulatory and audit requirements. This role requires co-ordination with stakeholders to fix the identified and reported compliance and control
Uita-te mai târziu06.06.2024 | Full-time | EYGet interviewed now, START your role on 1st of SEPTEMBERLocations Bucharest, Cluj-Napoca, Timisoara, IasiSchedule hybrid, full-timeImportant No previous work experience necessaryOur Audit teams analyze the data behind our clients’ businesses to give them, their investors and market regulators
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
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