Part-Time Clinical Research Coordinator - Impactful Trials

IQVIA; Toledo; Presencial; EUR 25.000 - 30.000; A tiempo parcial

Descripción de la vacante

IQVIA is seeking a Clinical Research Coordinator in Toledo for a part-time role of 20-24 hours per week. The position starts immediately and runs for approximately six months, supporting a clinical research site with prescreening, data management, patient screening, and study documentation.

The ideal candidate holds a life sciences degree or relevant clinical experience, strong IT skills, familiarity with trials and EDC systems, and English fluency.

Formación

• 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)

Responsabilidades

• Prescreening and Screening tasks
• Review charts from the site data base
• 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
• Processing lab samples
• Attend patient visits including ECG, vitals and potentially blood draws
• Performing data entry, quality checks, and resolving queries to ensure data accuracy and completeness
• Patient education
• Communicating with study monitors and responding to study-related inquiries
• Carrying out general administrative tasks related to the study

Educación

Bachelor’s degree in life sciences

Descripción del empleo

IQVIA is seeking a Clinical Research Coordinator in Toledo for a part-time role of 20-24 hours per week. The position starts immediately and runs for approximately six months, supporting a clinical research site with prescreening, data management, patient screening, and study documentation.

The ideal candidate holds a life sciences degree or relevant clinical experience, strong IT skills, familiarity with trials and EDC systems, and English fluency.