08.06.2024 | Full-time | ArcadisAre offering support in environmental analysiswith the final purpose to monitor and study levels of pollutants in the water and accountabilities Prepare, review and update environmental investigation and reports; Obtain, update and maintain plans, permits and standard operating procedures; Provide
Uita-te mai târziu08.06.2024 | 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 târziu08.06.2024 | Full-time | PharmiwebWith experts at study sites and with client representatives. Key Skills and Requirements University degree in a scientific discipline or health care. On-site monitoring experience. Good knowledge of clinical research regulatory requirements. Proficiency in MS Office. Excellent command of Romanian and English
Uita-te mai târziu08.06.2024 | Full-time | Bacău | Prysmian GroupToolsDesirable technical Knowledge SAP S4/HANA and ECC 6.0Knowledge of other SAP modules (APO, SD, MM, QM, PM, BW)BenefitsKinder GardenMeal ticketsVacation ticketsPrivate insuranceAdditional SkillsGeneral and specific Data Modeling capabilitiesResearch and self study attitudeForward thinking and strategic
Uita-te mai târziu08.06.2024 | Full-time | ParexelHungary, UK, Romania Croatia. This will be a home based role. Please note you must be fluent in main responsibility of the Site Contract Associate is the negotiation of study specific generic and country Clinical Site Agreement (CSA) templates with the Sponsor and support the PL
Uita-te mai târziu08.06.2024 | 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 târziu08.06.2024 | 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 târziu08.06.2024 | Full-time | HoneywellAnd a passion for their field of studyGood level of English language & any other European language is an important advantageAbility to work 30 -40 hours per week with flexibility
Uita-te mai târziu08.06.2024 | Full-time | Lugoj | HELLATeamCoordinating all quality-relevant activities e.g. Risk Assessment to prepare the sourcing. Checking whether the manufacturing feasibility study is available and whether supplier locations and processes are releasedYOUR QUALIFICATIONSTechnical University degree in electrical or mechanic's mum 1 year
Uita-te mai târziu08.06.2024 | Full-time | PharmiwebResolution Collaborating with experts at study sites and with client representatives Qualifications University degree in scientific discipline or health care At least 2.5 years of on-site monitoring experience Good knowledge of clinical research regulatory requirements Very good computer skills including MS
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