10.06.2024 | Full-time | PSIDepartmentQualificationsAround 1-3 years of clinical trials erably at least 1-year of industry experience in vendor management, proposal development, clinical trial operations, or business development working alongside or managing vendorsGood proficiency in MS Office applicationsC1 level in English languageAn
Uita-te mai târziu10.06.2024 | Full-time | IQVIAEstablish and agree on project planning and project timelines. Ensure monitoring measures are in place and implement contingency plan as rm team members of completion of regulatory and contractual documents for individual ew, track and follow up the progress, the approval and execution
Uita-te mai târziu10.06.2024 | Full-time | Thermo Fisher ScientificAnd internal/external stakeholdersWorking on project work and initiatives for process improvement as required RequirementsEducation and ExperienceDegree in pharmacy, life science or related field0 - 1 years’ clinical monitoring experienceFluency in English and RomanianKnowledge, Skills
Uita-te mai târziu10.06.2024 | Full-time | IQVIAJob OverviewThe Clinical Supply Chain Manager is responsible for managing the strategic planning and execution of a program of assigned clinical supply chain projects. The Clinical Supply Chain Manager will support the ongoing development and optimization of the Clinical Trial Supplies department
Uita-te mai târziu10.06.2024 | Full-time | Aspen MedicalTo practice nursing Certifications in BLS, ACLS, PHTLS, or equivalent Strong clinical skills and knowledge of medical procedures Excellent communication and interpersonal skills Contract Details - Contract duration 3+ years - Paid leave, accommodation, and per diem provided - Estimated starting date Middle
Uita-te mai târziu10.06.2024 | Full-time | Herz- und Diabeteszentrum Nordrhein-WestfalenInfrastructure, we are looking for an IT System Administrator PACS (m/f/d) to support the Clinical Systems and Development team. Your tasks at the HDZ NRW Design, coordination, implementation, monitoring and administration of the IT infrastructure with a focus on imaging systems including the corresponding
Uita-te mai târziu07.06.2024 | Full-time | Craiova | 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 | 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 târziu06.06.2024 | Full-time | PharmiwebRelated problems and prioritize workload for self and team You have previous clinical research monitoring experience (including pre-study, initiation, routine monitoring and closeout visits). Fluent Romanian and English Fortrea is actively seeking motivated problem-solvers and creative thinkers who share
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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