Research support technician - Clinical Trials Unit

Descrizione

Research support technician - Clinical Trials Unit Sintesi in italiano (traduzione automatica): L'organizzazione internazionale cerca un Tecnico di ricerca per la sua Unità di Sperimentazione Clinica. Il candidato selezionato avrà il compito di coordinare le attività tra ricercatori, pazienti e personale infermieristico, organizzando visite di avvio, screening e chiusura. Sarà responsabile della preparazione della documentazione necessaria e della gestione dei documenti personali dei ricercatori. Inoltre, parteciperà a riunioni virtuali e in presenza, gestendo anche la programmazione degli appuntamenti dei pazienti e l'organizzazione dei test clinici. È richiesta una laurea in discipline scientifiche o affini, oltre a competenze nella gestione della documentazione e nella comunicazione con i vari attori coinvolti nelle sperimentazioni cliniche. The selected candidate will have the following functions: Coordination with researchers, patients, and nursing staff. Organization and attendance at initiation, screening, pre-screening, and closing visits. Preparation of the necessary documentation for each visit. Organization of monitoring schedules and support for monitors on the day of their visits. - Preparation of informed consent forms and study documentation for researchers, ensuring they have it available in their office on the day of the visit. Management and updating of each researcher's personal documents and the research team's own records; and preparation of documents for each study. - Attendance at virtual and in-person meetings: training sessions and meetings with the sponsor. Maintenance of the researcher's file for each study, including both studies with patients and those in which they were not involved. Implementation of new studies: management of essential documentation. Management and updating of hospital documents: laboratory reference ranges, calibration certificates for all equipment used with patients participating in a study, laboratory certificates, primary care certificate, etc. Maintenance of internal records, calendars, and schedules: recording all patient visits, scheduled monitoring, initial, closing, and screening visits, etc. Management of patient appointments. Submitting and requesting appointments, adjusting them to the schedule required by the protocol. Scheduling and organizing patient visits, as well as daily organization of clinical tests and nursing procedures: preparing nursing notes, reviewing the protocol to obtain all necessary data, preparing blood collection tubes, assisting patients in completing quality of life questionnaires and using patient devices, etc. Processing samples and sending them to the sponsor. Assistance and support during inspections and audits. Any other function that, within the scope of their responsibilities, may be entrusted to them by the research staff responsible for the Trials or the person responsible for Clinical Trials of the Foundation. Annuncio in inglese. Fonte: Euraxess (Commissione europea).