Research Nurse For The Clinical Research Support Unit

buscojobs España; Valladolid; Presencial; EUR 30.000 - 40.000; Jornada completa

Descripción de la vacante

Une entreprise leader dans le domaine des sciences médicales recherche un coordonnateur d'essais cliniques pour rejoindre son équipe de recherche. Le candidat retenu assurera le soutien complet aux soins des patients et gérera efficacement toutes les phases des essais cliniques. Ce poste est idéal pour une personne ayant de solides compétences organisationnelles et une formation dans les sciences médicales.

Formación

• Expérience en gestion des essais cliniques et pharmacovigilance.
• Compétences organisationnelles et de communication.
• Capacité à travailler avec des équipes de recherche.

Responsabilidades

• Gestion des procédures de soins infirmiers et tests complémentaires.
• Coordination des essais cliniques et communication entre les services médicaux.
• Facilitation du recrutement des patients et suivi des contrôles.

Conocimientos

Gestion des essais cliniques

Pharmacovigilance

Coordination

Soutien aux patients

Educación

Titre académique dans les sciences médicales

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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