10 Best pre requisitos Jobs in Oviedo (July 2026)

Research support technician - Clinical Trials Unit

6 days ago

Oviedo

Organisation/Company Instituto de Investigación Sanitaria del Principado de Asturias Research Field Medical sciences Researcher Profile Other Profession Positions Bachelor Positions Application Deadline 23 Jul 2026 - 23:59 (Europe/Madrid) Country Spain Type of Contract Permanent Job Status Full-time Hours Per Week 37.5 Is the job funded through the EU Research Framework Programme? Not funded by a EU programme Is the Job related to staff position within a Research Infrastructure? No Inscríbase rápido, consulte la descripción completa desplazándose hacia abajo para conocer todos los requisitos de este puesto. Offer Description 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. xcskxlj, • 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. #J-18808-Ljbffr

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