Research Nurse for the Clinical Research Support Unit

Institut de Recerca Biomèdica de Lleida, Fundació Dr. Pifarré (IRBLleida); Badajoz; Presencial; EUR 30.000 - 50.000; Jornada completa

Descripción de la vacante

A leading biomedical research institute in Spain seeks a skilled researcher to join its Clinical Research Support Unit. The candidate will primarily be responsible for managing clinical trials, coordinating patient care, and ensuring compliance with protocols. This full-time permanent position promises a dynamic work environment and an opportunity to contribute significantly to clinical studies.

Formación

• Bachelor's degree required.
• Experience in clinical trials is an asset.
• Strong organizational and coordination skills are essential.

Responsabilidades

• Control and management of nursing procedures and complementary tests.
• Comprehensive support for patient care and scheduling.
• Coordination of clinical trials and managing audits.

Conocimientos

Pharmacovigilance

Patient Care

Clinical Trial Coordination

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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