Clinical Trials Associate

Descripción del empleo

About the Company

I’m currently working with a CRO based in Spain for an exciting CTA role on a hybrid model.

About the Role

The idea is for the individual to transition from a CTA to a junior CPM. In this role, you would support clinical study teams with Trial Master File (TMF) management, document tracking, regulatory submissions, and general study coordination activities to ensure compliance and smooth trial execution.

Responsibilities

• Support clinical study teams with Trial Master File (TMF) management
• Document tracking
• Regulatory submissions
• General study coordination activities to ensure compliance and smooth trial execution

Qualifications

• 4-5 years as a junior - mid level CTA

Required Skills

• Smartsheet management experience

Información extra

Status

Activa

Estudios requeridos

E.S.O

Localización

Vitoria-Gasteiz

Tipo de contrato

Trabajo estudiantes

Publicado el

09-05-2026

Carnet de conducir

No

Vehículo

No

Carta de motivación

No

Idiomas

Español