Offer DescriptionAbout the research groupThe clinical research support unit (Unitat de Suport a la Recerca Clínica-USRC) was established in 2018 as part of the Clinical Research Department at IDIBELL to provide support to the researchers at Hospital Univeritari de Bellvitge (HUB) for conducting clinical trials research studies.
Currently the unit is engaging more than 80 studies of different therapeutic areas through scientifico-tecnic, administrative and execution support.About the roleWe are looking for a full-time study nurse and study coordinator to contribute to the development and implementation of different research projects and to work in a multidisciplinary team being the site nurse and site study coordinator responsible for the day-to-day of clinical studies carried out at Hospital Universitari de Bellvitge.
The research staff will work and interact with a multidisciplinary team including physicians, research coordinators, and pharmacists.Main tasks and responsibilities:Monitor the participants' medical condition and schedule and conduct research protocol follow-ups.Provide information to potential participants in clinical research studies.Selection, inclusion and follow-up of patients in clinical research studies.Collection of blood and other biological samples from patients participating in clinical research studies following all research procedures within approved study protocols.Handle biological samples: centrifuge, freezing, shipping to central laboratories, etc.Complete patient assessment (vital signs, ECG recording, etc).Carefully monitor the patient during the administration of the investigational drug.Participate in the meetings and activities of the Research Group.Coordinate clinical research studies in different therapeutic areas:Responsible for the researcher's archive.Support to Investigators to carry out study procedures.Provide guidance on the organization of all the clinical study.Review and update the regulatory submission documents as required by the protocol.Coordinate study visits and medical tests.Maintain the investigator site file.Data entry: In the eCRF from the different source documents.Collect data as required by the protocol.
Assure timely completion of Case report Forms.eCRF data entry and queries resolution.Job requirementsProfessional experience:Previous experience in a similar position.Education and training:Bachelor's Degree in nursing.Technical soft skills:Knowledge of medical terminology.Problem solving.Proactive diligent.Motivation, initiative and ability to learn.Good organizational skills with attention to detail.Collaborative and teamwork skills.Good IT competence: MS Windows and Office applications.Good communication and teamwork skills.High motivation and initiative.Results orientation.Languages:Good command of the English language.Catalan and Spanish spoken and written.We will value, but not required:Knowledge of the ethical and legal norm that regulates clinical research.Flexibility and adaptability to different therapeutic areas.Knowledge / experience in the national health system.Command of eCRF and Clinical trial management platforms.What do we offer:No.
of positions: 1.Estimated start date: 16/12/2024.Contract duration: permanent linked to projects.Estimated annual gross salary: 26.380 euros annual gross.Multicultural team with a friendly international work environment.Flexible working schedule.Possibility to work some days remotely - Teleworking.26 working days of holiday per year.System of accumulated hours for employees, from 88 to 104 hours depending on the year (11 to 13 working days), to attend to personal matters.Paid leave package.Benefits of constant training are offered.We promote diverse and inclusive conditions, free from discrimination.Deadline: Please submit your application by 13/12/2024.
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