Clinical Research Assoicate

Job Description

We are seeking a highly skilled Clinical Research Associate (CRA) to lead performance and compliance for assigned protocols and sites within Portugal - Zona Norte . Under the oversight of the CRA Manager, you will serve as the primary site contact throughout all phases of clinical studies, ensuring rigorous adherence to ICH/GCP, local regulations, our company policies and procedures, quality standards, and adverse event reporting requirements.

You will take ownership of allocated sites, actively collaborate in expanding our clinical research territory by identifying and developing new sites and contribute as a subject matter expert on monitoring processes and systems across internal workstreams.

The person must live in north of Portugal (Porto).

What you will do:  

• Build and sustain strong relationships with investigative sites across all trial phases.
• Perform site management and monitor...