Clinical Trial Documentation & TMF Coordinator

IQVIA; Madrid; Presencial; EUR 24.000 - 36.000; Jornada completa

Descripción de la vacante

IQVIA is seeking a Clinical Trials Assistant to support daily TMF activities, document control, and coordination with CRAs and RSU teams to keep study files complete and compliant.

You will help prepare, file, and archive clinical documents, assist with study file reviews, and handle CRF tracking and query resolution under project timelines.

Requirements include a life sciences degree, at least 1 year of CT assistant experience, and fluent English and Spanish.

Formación

• Bachelor's degree in life sciences or related field preferred.
• At least 1 year of experience as Clinical Trials Assistant.
• Strong written and verbal communication in English and Spanish.

Responsabilidades

• Assist CRAs and RSU with updating and maintaining TMF and documents.
• Prepare, handle, file and archive clinical documents and reports per SOPs.
• Conduct periodic reviews of study files for completeness.
• Support distribution of Clinical Trial Supplies and tracking information.
• Track Case Report Forms (CRFs), queries and data flow.

Conocimientos

Time management

Communication skills

Bilingual English/Spanish

Educación

Bachelor's degree in life sciences

Herramientas

Microsoft Word

Excel

PowerPoint

Descripción del empleo

IQVIA is seeking a Clinical Trials Assistant to support daily TMF activities, document control, and coordination with CRAs and RSU teams to keep study files complete and compliant.

You will help prepare, file, and archive clinical documents, assist with study file reviews, and handle CRF tracking and query resolution under project timelines.

Requirements include a life sciences degree, at least 1 year of CT assistant experience, and fluent English and Spanish.