2024. 06. 19. | Teljes munkaidõ | Budapest | ProclinicalAbstraction, extraction, archiving, collection, entry, validation, queries, analysis, storage, privacy, transmission, workflows, and discrepancy management.- Designing, building, and testing databases.- Reconciling severe adverse events (SAEs).- Tracking study metrics.- Ensuring quality control and assurance
Nézze később2024. 06. 19. | Teljes munkaidõ | Budapest | IQVIAAvailable in accordance with the project requirementsInitiate packaging campaigns with the assigned vendor and provide oversight to ensure on-time deliverySetup, monitor, and where necessary, update study assigned Interactive Response Technology (IRT) systems to ensure study inventory is effectively
Nézze később2024. 06. 16. | Részmunkaidõ | Budapest | SanofiWho want to gain useful work experience in an international organisation and become part of an inspiring, young 'll find the right position for you, whatever your field of study, as Sanofi sites offer a variety of internships for students who want to t the jobPreparation of draft
Nézze később2024. 06. 16. | Részmunkaidõ | Budapest | SanofiOf opportunities for students who want to gain useful work experience in an international organisation and become part of an inspiring, young 'll find the right position for you, whatever your field of study, as Sanofi sites offer a variety of internships for students who want to t the jobClosely
Nézze később2024. 06. 12. | Teljes munkaidõ | Budapest | haysThe data to develop sales reports according to the business users’ needs. They understand the sales mechanism, processes, and trends behind the data and have the creativity to represent it in an easy-to-understand form. - Study system capabilities and current practices, evaluate data output requirements
Nézze később2024. 05. 23. | Teljes munkaidõ | Budapest | haysWith study protocols - Develop and implement a relevant clinical trial data management plan - Work with scientists and relevant personnel to develop data-related SOPs that allow for centralized and remote data monitoring, tracking, and verification of all aspects of clinical trials. - Import existing data
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