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Clinical Research Coordinator / Study Nurse - Villamartin

TN Spain

Cádiz

Presencial

EUR 24.000 - 36.000

A tiempo parcial

Hace 26 días

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Descripción de la vacante

Una empresa líder en la industria busca un Coordinador de Investigación Clínica / Enfermero de Estudio para unirse a su equipo en Villamartín. En este emocionante rol a tiempo parcial, serás responsable de apoyar un estudio de investigación clínica, garantizando un entorno de estudio seguro y cumpliendo con las políticas de salud y seguridad. Te involucrarás en diversas tareas administrativas para asegurar el buen funcionamiento del ensayo clínico, incluyendo la gestión de documentos y la coordinación de actividades logísticas. Si tienes una licenciatura en ciencias de la vida y experiencia en entornos clínicos, esta podría ser la oportunidad perfecta para ti.

Formación

  • Licenciatura en ciencias de la vida o experiencia laboral relevante.
  • Experiencia en la realización de ECG y toma de signos vitales.

Responsabilidades

  • Mantener protocolos de estudio y formularios de informe de caso actualizados.
  • Coordinar actividades logísticas para los procedimientos del estudio.

Conocimientos

Conocimientos de ensayos clínicos
Habilidades interpersonales
Organización y atención al detalle
Competencia en IT
Fluidez en español e inglés

Educación

Licenciatura en ciencias de la vida
Experiencia laboral relevante en un entorno clínico

Herramientas

MS Windows
MS Office (Access, Outlook, Excel, Word)
Sistemas de captura de datos electrónicos (EDC)

Descripción del empleo

Social network you want to login/join with:

Client:

IQVIA

Location:
Job Category:

Other

EU work permit required:

Yes

Job Views:

2

Posted:

25.04.2025

Expiry Date:

09.06.2025

Job Description:

Are you looking for an opportunity to work with an industry-leading company? IQVIA is currently recruiting for a Clinical Research Coordinator / Study Nurse to support a site in Villamartin.

This part-time role is for 24 hours per week and is expected to last approximately 1 year. The successful candidate will be responsible for supporting a clinical research study and maintaining a safe study environment in accordance with health and safety policies, under the direction and delegation of the Principal Investigator.

As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support the clinical trial team and ensure the smooth running of the clinical trial, including:

  • Maintaining up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents
  • Performing ECG and vital signs
  • Planning and coordinating logistical activity for study procedures according to the study protocol
  • Data entry, data quality checking, and query resolution to ensure adherence to study protocol and quality control for content accuracy and completeness
  • Assisting in study enrollment by recruiting, screening, and orienting volunteers according to the study protocol
  • Correctly managing custody of study drug according to site standard operating procedures
  • Coordinating with study monitor on study issues and effectively responding to monitor-initiated questions
  • Ordering and maintaining study supplies

We are looking for candidates with:

  • BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting, e.g. clinical research coordinator, Research Assistant, nurse, medical assistant, other medical profession
  • Experience conducting ECG and taking vital signs
  • Good knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules
  • Basic knowledge of medical terminology
  • Strong IT competence, skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word
  • Excellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers and clients
  • Good organizational skills with the ability to pay close attention to detail
  • Fluent Spanish and English language skills

If this sounds like the perfect opportunity for you, please apply now!

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