Offer Description
Study Nurse - USRC (Non-clinical staff) - Replacement position Ref.
24-150_SS_MG
About 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 coordinator to contribute to the development and implementation of different research projects and to work in a multidisciplinary team being 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.Handling of biological samples: centrifuge, freezing, shipping to central laboratories, etc.Complete patient assessment (vital signs, ECG recording, etc).Careful monitoring of the patient during the administration of the investigational drug.Participation in the meetings and activities of the Research Group.Coordination of 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.Reviews and updates on the regulatory submission documents as required by the protocol.Coordinate study visits and medical tests.Investigator site file maintenance.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 experienceAt least one year in a similar position.
Education and trainingDegree in Life Sciences.Bachelor's Degree in nursing.Technical & soft skillsKnowledge of medical terminology.Problem solving.Proactive & diligent.Motivation, initiative and ability to learn.Good organizational skills with the ability to pay close 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.LanguagesGood command of the English language; Catalan and Spanish spoken and written.
We will value, but not requiredKnowledge 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 offerNo.
of positions: 1Estimated start date: as soon as possibleContract duration: Temporary contract to cover sick leaveEstimated annual gross salary: € 28.000You will be part of a multicultural team with a fun loving and friendly international work environment.Flexible working schedule.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 offer and promote diverse and inclusive conditions.Deadline: Please submit your application by 16/12/2024
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