2024. 04. 26. | Teljes munkaidõ | Budapest | IQVIAFor clinical trials by serving as Medical Monitor for studies conducted by IQVIA Biotech Clinical on behalf of sponsor companies. The principal function of a Medical Monitor is to serve as primary contact for the sponsor medical team and to serve as front line medical resource to support the project team
Nézze később2024. 04. 26. | Teljes munkaidõ | Budapest | SanofiThe acceleration of the digitalization of R&D data landscape by building state-of-the-art Data fabric and delivering AI-powered Data Products across R&D functions. As part of this transversal team, Digital Clinical Data Product teams is delivering new Clinical Data products to transform Clinical trials, accelerate
Nézze később2024. 04. 26. | Teljes munkaidõ | Budapest | ClarioAnd hands-on experience in Clinical Trials who have benefitted from utilising eCOA, ePRO, IRT, RTSM, eConsent, and other innovative eClinical we offerCompetitive CompensationAttractive Benefits (security, flexibility, support and well-being)Engaging Employee ProgramsRemote/Hybrid
Nézze később2024. 04. 26. | Teljes munkaidõ | Budapest | VodafoneOf journal entries, fixed asset or inventory accounting, preparation of trial balance or financial statements, cost accounting, bank account reconciliation, profit and loss reportDrafts segments of statements and reportsHandles assignments involving analysis of data. Prepares reports and analyses
Nézze később2024. 04. 26. | Teljes munkaidõ | Budapest | FortreaAnd ResponsibilitiesMain Point of Contact for assigned protocols and link between Country Operations and clinical trial teamResponsible for project management of the assigned studies actively plans, drive and track execution and performance of deliverables/timelines/results to meet country commitments from feasibility
Nézze később2024. 04. 26. | Teljes munkaidõ | Budapest | ClarioContinue to innovate technology that will shape the future of clinical io is committed to providing an inclusive workplace that welcomes diversity and equal opportunity. We encourage all qualified candidates who are passionate about sustainability, ethical business, and making a positive impact
Nézze később2024. 04. 26. | Teljes munkaidõ | Budapest | IQVIAOr more programs enabling planning, coordination, and timely delivery of complete, high quality and reliable clinical trial data for regulatory approval and market acceptanceLead a Functional Department of Data Management staff. Size of team could vary from 15-40, and may be a first-line or second-line
Nézze később2024. 04. 26. | Teljes munkaidõ | Budapest | ParexelMV) and termination visits (TV) at assigned clinical sites and generate visit/contact d relationships. Oversee integrity of the study and utilize problem-solving skills to promote rapport with the site and ect patients. Review the performance of the trial at designated sites
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Napi új bejegyzéseket kaphat e-mailben a Clinical Trial Assistant Budapesti Kerület.