09 Dec | Institut D'Investigació Biomédica De Bellvitge (Idibell) | L'Hospitalet de Llobregat
Study Nurse – USRC (Non-clinical staff) - Replacement position
Ref. 24-150_SS_MG
About the research group
The 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 Universitari 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 role
We 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.Review and update 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 different source documents.Collect data as required by the protocol. Assure timely completion of Case report Forms.eCRF data entry and queries resolution.Job requirements Professional experience
- At least one year in a similar position.
Education and training
- Degree in Life Sciences
- 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 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: as soon as possible
- Contract duration: Temporary contract to cover sick leave.
- Estimated annual gross salary: € 28.000
- You will be part of a multicultural team in a friendly international work environment.
- Flexible working schedule.
- 26 working days of holiday per year.
- System of accumulated hours for employees.
- Paid leave package.
- Benefits of constant training are offered.
- Commitment to diversity and inclusion.
Deadline: Please submit your application by 16/12/2024.
Data protection notice
In compliance with the obligations established in the General Regulation of Data Protection (RGPD), the Institut d'Investigació Biomèdica de Bellvitge (IDIBELL) will process your personal data to apply for the position and maintain communication concerning the status of the candidature. You can find more information in our Privacy Policy at https://idibell.cat/en/privacy-policy-2/.
Our institute
IDIBELL is a research center that integrates the biomedical research of the Bellvitge University Hospital (HUB), the Catalan Institute of Oncology (ICO), and the University of Barcelona in the Bellvitge Campus (UB), focusing on cancer, neuroscience, translational medicine, and regenerative medicine.
Observations
The 'HR Excellence in Research' award represents IDIBELL's commitment to the implementation of Human Resources policies that oversee the attracting and development of talent in an open, transparent, and merit-based manner.
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