Clinical Trial Coordinator - TMF & Compliance (Hybrid)

IQVIA Argentina; Ciudad de México; Híbrido; MXN 167.000 - 279.000; Jornada completa

Descripción de la vacante

IQVIA in Mexico City is seeking an administrative support professional to assist CRAs and RSU with Trial Master File updates and regulatory documentation. The role involves filing, archiving, and coordinating clinical documents to keep projects on track.

The candidate should have a Life Science degree and 6 months to 1 year of clinical research exposure, with strong English communication and MS Office skills. Hybrid office-based work is required.

Formación

• Written and verbal communication in English clearly and professionally.
• Familiarity with TMF and regulatory document handling.
• SOP-compliant archiving and filing.

Responsabilidades

• Update and maintain Trial Master File (TMF) and related systems.
• Prepare, handle, file and archive clinical documents per SOPs.
• Review study files for completeness on a periodic basis.
• Track Clinical Trial Supplies and maintain task records.
• Monitor CRFs, queries and data flow with the clinical team.
• Serve as central contact for project communications and documentation.
• May join CRAs on site visits after training.

Conocimientos

English language

MS Word

MS Excel

PowerPoint

Time management

Organizational skills

Communication skills

Educación

Bachelor's degree in Life Science

Descripción del empleo

IQVIA in Mexico City is seeking an administrative support professional to assist CRAs and RSU with Trial Master File updates and regulatory documentation. The role involves filing, archiving, and coordinating clinical documents to keep projects on track.

The candidate should have a Life Science degree and 6 months to 1 year of clinical research exposure, with strong English communication and MS Office skills. Hybrid office-based work is required.