07.06.2024 | Full-time | PharmiwebFor clinical studies in phases I - IV, ensuring adherence to applicable regulations and principles of ICH-GCP. Responsibilities will include Conduct a variety of different site visits. This is inclusive of selection, initiation, monitoring and close-out visits Supporting the development of a subject
Uita-te mai târziu07.06.2024 | 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 | Chronos ConsultingJob Description Our client is a global leader in non-invasive neurosurgical treatments. The company is dedicated to improving patient lives by collaborating with physicians, medical institutions, academic researchers and regulatory bodies around the are currently looking for a Sales
Uita-te mai târziu06.06.2024 | Full-time | Craiova | Antal InternationalBalance sheets and profit & loss statements. Assess and evaluate team performance. Ensure financial documents are maintained in accordance with current laws and regulations. Review and interpret balance sheets, profit and loss accounts, consolidated financial statements, and other accounting documents
Uita-te mai târziu06.06.2024 | 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 | 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 | 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 | 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 | 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 | 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
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