Descripción de la oferta
University Mid-Level Research Support Officer – Group CPara presentar una candidatura, simplemente lea la siguiente descripción del puesto y asegúrese de adjuntar los documentos pertinentes.Reference number: HR-26/031Start Period: Monday, July 6, 2026End Period: 23:59 p.M. on Thursday, July 16, 2026Required requirements:Hold a Bachelor's Degree in Human Nutrition and DieteticsSix months of experience supporting nutrition/health research projects, preferably in intervention studies with participants.Main functions to be developed:Collaboration, under the direct supervision of the Principal Investigator (PI), in the material execution of the nutritional assessment tests of the patients included in the clinical studies (taking anthropometric measurements, completing nutritional screening tests and recording dietary follow-up).Support in the application and monitoring of nutritional interventions prescribed by the PI in the context of liver disease studies.Completion of the formal collection and dumping of dietary data through the supervised administration of 24-hour reminders, frequency questionnaires and food records, without autonomous diagnostic capacity.Collaboration in administrative and support tasks for the preparation of draft research protocols in nutrition and hepatology under the guidelines of the project manager.Transfer and maintenance of clinical data in electronic data collection notebooks (eCRF), ensuring their transcription according to the instructions received.Collaboration in the formal review of databases for the detection of inconsistencies, communicating the queries to the IP or senior staff for their resolution.Trial Master File (TMF) management and archiving.Monitoring assistance: Provide logistical and administrative support during monitoring visits and audits with constant supervision by the IP.Facilitate communication channels and exchange of technical documentation between principal investigators, monitors (CRA) and the rest of the work team.Collaboration in the preparation, organization and sending of the necessary documentation intended for the Ethics Committees for Research with medicines (CEIm).Support tasks assigned strictly following standardized work procedures, Good Clinical Practice (ICH-GCP) regulations, AEMPS guidelines and RD 1090/2015, under the direction of the PI.Support in data transcription, information organization and preparation of administrative support for the preparation of reports, databases and presentation of preliminary results. xqbhyrx In addition to the above, other technical and operational support tasks may be carried out, always within the functions corresponding to Group C of University Graduate/a in Research Support.Contact: 976 71 68 18 / #J-18808-Ljbffr
