Part-Time Clinical Research Coordinator — Toledo

IQVIA Argentina; Alía; Presencial; EUR 21.000 - 39.000; A tiempo parcial

Descripción de la vacante

IQVIA is recruiting a Clinical Research Coordinator to support a study site in Toledo. This part-time role offers 20-24 hours per week with an immediate start and an expected duration of about six months.

The candidate will prescreen, screen, review site charts, maintain study documentation, assist with informed consent, coordinate study procedures, process lab samples, and support data entry and quality checks.

Formación

• Bachelor's degree in life sciences or equivalent education and experience.
• Solid understanding of clinical trials and familiarity with study protocols, consent forms, and schedules.
• Good knowledge of medical terminology.
• Must have at least 2 years experience as a Clinical Research Assistant, Research Nurse or CRC at a clinical trial site.
• Fluency in English and strong interpersonal skills.

Responsabilidades

• Prescreening and Screening tasks.
• Review charts from the site data base.
• Maintain and update study documentation including protocols, CRFs, and EDC systems.
• Support patient screening and enrollment including informed consent and privacy documentation.
• Coordinate logistical activities for study procedures per protocol.
• Process lab samples.
• Attend patient visits including ECG, vitals and potentially blood draws.
• Data entry, quality checks, and resolve queries to ensure data accuracy.
• Patient education.
• Communicate with study monitors and respond to inquiries.
• Carry out general administrative tasks related to the study.

Conocimientos

MS Office

IT skills

Interpersonal skills

Organizational skills

English fluency

Communication skills

Educación

Bachelor's degree in life sciences

Herramientas

MS Office

Descripción del empleo

IQVIA is recruiting a Clinical Research Coordinator to support a study site in Toledo. This part-time role offers 20-24 hours per week with an immediate start and an expected duration of about six months.

The candidate will prescreen, screen, review site charts, maintain study documentation, assist with informed consent, coordinate study procedures, process lab samples, and support data entry and quality checks.