Clinical Trials Support Specialist

IQVIA; Barcelona; Híbrido; EUR 26.000 - 38.000; Jornada completa

Descripción de la vacante

IQVIA in Spain seeks a Clinical Trials Assistant to support daily TMF activities and document control alongside CRAs and RSU. You will help prepare, file, and archive clinical documentation, ensuring compliance with SOPs and regulatory standards.

The role requires coordinating study materials, tracking CRFs, and maintaining effective communication across teams. Ideal candidates have a life sciences degree with 1+ year of trial experience, and fluent English/Spanish.

Formación

• Bachelor’s or higher in life sciences preferred.
• At least 1 year of experience as Clinical Trials Assistant.
• Fluent in English and Spanish; strong written and verbal skills.
• Proficient in Word, Excel, and PowerPoint; regulatory awareness (GCP/ICH).

Responsabilidades

• Assist CRAs and RSU with TMF updates and document control.
• Prepare, file, and archive clinical documents per SOPs.
• Review study files for completeness on a periodic basis.
• Help with Clinical Trial Supplies tracking and CRF data flow.
• Serve as central point of contact for project communications.
• Support on-site visits for monitoring after training.

Conocimientos

Time management

Organizational skills

Written and verbal communication

Fluent in English & Spanish

Educación

Bachelor's degree in life sciences

Herramientas

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

Descripción del empleo

IQVIA in Spain seeks a Clinical Trials Assistant to support daily TMF activities and document control alongside CRAs and RSU. You will help prepare, file, and archive clinical documentation, ensuring compliance with SOPs and regulatory standards.

The role requires coordinating study materials, tracking CRFs, and maintaining effective communication across teams. Ideal candidates have a life sciences degree with 1+ year of trial experience, and fluent English/Spanish.