Research Nurse for the Clinical Research Support Unit

Institut de Recerca Biomèdica de Lleida, Fundació Dr. Pifarré (IRBLleida); Jaén; Presencial; EUR 30.000 - 45.000; Jornada completa

Descripción de la vacante

A leading biomedical research institute in Spain is seeking a full-time Clinical Research Support Unit member. The role involves managing nursing procedures, supporting patient care, and coordinating clinical trials. Ideal candidates will have a Bachelor's degree and experience in clinical settings.

Formación

• Bachelor's degree required.
• Experience in clinical research or healthcare preferred.
• Strong organizational and communication skills.

Responsabilidades

• Control and management of nursing procedures and complementary tests.
• Comprehensive support for patient care.
• Coordination of clinical trials and communication with researchers.

Conocimientos

Patient care

Pharmacovigilance

Clinical trial coordination

Data management

Educación

Bachelor's degree

Descripción del empleo

Research Field : Medical sciences » Health sciences

Researcher Profile : Other

Profession : Positions Bachelor

Country : Spain

Application Deadline : 22 May 2025 - 14 : 00 (Europe / Madrid)

Type of Contract : Permanent

Job Status : Full-time

Is the job funded through the EU Research Framework Programme? Not funded by a EU programme

Is the Job related to staff position within a Research Infrastructure? Yes

Offer Description

The selected candidate will join the Scientific-Technical Service (SCT) Clinical Research Support Unit (USIC) of IRBLleida and will carry out the following tasks :

• Control and management of nursing procedures and complementary tests according to each protocol.
• Comprehensive support for patient care.
• Scheduling of patients and tests.
• Pharmacovigilance : management of adverse events.
• Functions of coordination of clinical trials :
• Participate in the selection of the centre and the research team.
• Participate in the evaluation of the feasibility of the study, analysis of the circuits and technical needs, spaces and personnel of each clinical trial.
• Conducting meetings with researchers and facilitating communication between the medical services involved in the study and the external parties involved.
• Maintenance of necessary files : researcher, promoter, pharmacy.
• Facilitate the recruitment process and obtaining informed consent.
• Coordination of visits and follow-up controls.
• Management of possible audits.
• Contact with monitors and preparation of documentation for external monitoring.
• Recording of data in the data collection logbook, resolution of complaints and monitoring.
• As well as any other task that is entrusted to them according to their training and skills.

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