Clinical Trials Study Nurse - Vascular Risk Unit (35h/ Week)

Clinical Trials Study Nurse - Vascular Risk Unit (35h/ Week)

REF. 26-162_SS_AG

About the research group

The Vascular Risk Unit, attached to the Internal Medicine Service of Bellvitge University Hospital, boast over 25 years of experience. This group is included in the Research Groups of the Bellvitge Biomedical Research Institute (IDIBELL), linked to the Bellvitge University Hospital, and also integrated in the Center for Biomedical Research in Network of the Physiopathology of Obesity and Nutrition (CIBERobn) dependent on the Carlos III Health Institute (Ministry of Economy and Competitiveness). Our primary objective is to investigate the determinants of dyslipidemia, hypertension, obesity, diabetes and cardiovascular diseases to improve the cardiovascular health of the population.

About the role

We are looking for study nurse to contribute to the development and implementation of different research projects and to work in a multidisciplinary team being the site nurse of clinical studies carried out at the Vascular Risk Unit. The research staff will work and interact with a multidisciplinary team including physicians, research coordinators, and nutricionists.

Main tasks and responsibilities: Applicants should be able to monitor the participants’ medical condition and schedule and conduct re-search protocol follow-ups. Information to potential participants in clinical research studies. 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. Data entry: In the eCRF from the different source documents:

- Collect data as required by the protocol. Ensure timely completion of Case report Forms.

- eCRF data entry and query resolution.

Job requirements

Professional experience

• Previous experience in a similar position, preferably in clinical research will be valued.

Education and training

• Bachelor's Degree in Nursing.

Technical & soft skills

• Knowledge of medical terminology.
• Strong problem-solving abilities.
• Proactive & diligent.
• High 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
• Results orientation
• Adaptability and flexibility.

Languages

• Good command of the English language
• Fluency in Spanish and Catala

We will value, but not required

• Knowledge of the ethical and legal regulations governing clinical research (GCP).
• Command of eCRF and Clinical trial management platforms.
• Experiencie collaborating in clinical trials focused of Nutrition, Cardiovascular Risk Factors, and Lipid Metabolism,
• Experiencie entering research data into eCRF (CRFin eMedidata, Clintrack, )
• Basic knowledge of Statistical analysis
• Experence using SAP of HUB software.

What do we offer

• No. of positions: 1
• Estimated start date: As soon as possible
• Contract duration: Permanent by project
• Estimated annual gross salary: 31.497,78€
• You will be part of a multicultural team. We have a fun loving and friendly international work environment.
• Flexible working schedule - We know you have a life outside of work and we will work with you to make sure it's kept that way.
• 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. Applicants are made free from any discrimination. Specifically IDIBELL works to improve gender equality in all areas with the aim of achieving gender balance, but maintaining the most scrupulous respect to any choice at the level of gender identity. Please express yourself freely, safely and non-binarily, if that's the case.

Deadline: Please submit your application by 25/11/2026

Data protection notice

In compliance with the obligations established in the General Regulation of Data Protection (RGPD), which is the Regulation (EU) 2016/679 of the Parliament and of the Council, of April 27, 2016, and the Organic Law 3/2018, of December 5, Protection of Personal Data and guarantee of digital rights, it is reported that the Institut d'Investigació Biomèdica de Bellvitge (IDIBELL), CIF G58863317, with address Av. Granvia de l'Hospitalet, 199-203, 08908, L'Hospitalet de Llobregat, will process your personal data, as the controller, to apply for the position, maintain communication concerning the status of the candidature, to access the delivered CV; to compare that your data is in accordance with the offers announced by IDIBELL and to verify, where appropriate, that the information provided is accurate. You can find more information in our Privacy Policy at https://idibell.cat/en/privacy-policy-2/, request more information about the data processing carried out and exercise your rights of access, rectification, deletion, opposition, portability, limitation of processing by sending a request at email: dataprotection@idibell.cat. If you consider that you have not obtained satisfaction in exercising your rights, you may submit a claim to Catalan Data Protection Authority.

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), and the Viladecans Hospital (HV). The research focuses of IDIBELL are cancer, neuroscience, translational medicine and regenerative medicine. Research, innovation and society are the pivots on which researchers work every day in order to improve the quality of life of citizens.

Observations:

The 'HR Excellence in Research' award represents IDIBELL’s commitment to the implementation of Human Resources policies, which oversee the attracting and development of talent in an open, transparent, and based on personal merit, in alignment with the principles of the European Charter for Researchers and the Code of Conduct for the Recruitment Researchers (Charter and Code).

IDIBELL is committed to the principles of the Code of Conduct for the Recruitment of Researchers of the European Commission and the implementation of open, transparent and merit-based recruitment (OTMR).

• Bases de la convocatoria