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Clinical Research Coordinator

Trabajo disponible en: 45001, Toledo, Castilla - La Mancha, España
Empresa: IQVIA
Tiempo parcial puesto
Publicado en 2026-02-02
Especializaciones laborales:
  • Servicios Médicos
    Investigación clínica
  • Investigación/Desarrollo
    Investigación clínica
Descripción del trabajo
Clinical Research Coordinator – Toledo (Part-Time, 20-24hours/week)

Start Date:

immediately

Duration: until 30th of September 2026

IQVIA is currently recruiting a dedicated Clinical Research Coordinator to support a clinical research site in Toledo. This part-time position offers a unique opportunity to contribute to meaningful research in a collaborative and dynamic environment.

Key Responsibilities As a vital member of the site team, you will help ensure the smooth execution of the clinical trial by performing a range of administrative and clinical support tasks, including:

Maintaining and updating study documentation, including protocols, case report forms (CRFs), and Electronic Data Capture (EDC) systems

Supporting patient screening and enrollment, including handling informed consent and privacy documentation

Coordinating logistical activities for study procedures in line with the study protocol

Performing data entry, quality checks, and resolving queries to ensure data accuracy and completeness

Managing and shipping biological samples

Communicating with study monitors and responding to study-related inquiries

Help with patient recruitment, patient education and community outreach

Carrying out general administrative tasks related to the study

Your Profile We are looking for candidates who bring a combination of education, experience, and skills:

Bachelor’s degree in life sciences or equivalent education and/or relevant experience in a clinical or medical setting (e.g., clinical research coordinator, research assistant, nurse, medical assistant)
Solid understanding of clinical trials and familiarity with study protocols, consent forms, and schedulesgood knowledge of medical terminology

Strong IT skills, including proficiency in MS Office applications (Outlook, Word, Excel, Access)
Must have at least 1-2 years experience working as a Clinical Research Assistant, Research Nurse or Clinical Research Coordinator at a clinical trial site Excellent interpersonal and communication skills

Strong organizational skills and attention to detail

Fluency in Spanish and good command of English Why Join IQVIA?

At IQVIA, you will be part of a global team that is advancing healthcare through data, technology, and human science. We offer a supportive work environment, impactful projects, and the opportunity to make a real difference.

Interested?

If this sounds like the right opportunity for you, we encourage you to apply today.
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