Company Description
Our client is a Global CRO currently supporting various Pharmaceutical & Biotech companies globally. They offer a full service solution encompassing clinical & non-clinical development, peri-approval & market access. They are currently seeking a CRA sponsor dedicated home based in Sevilla.
Job Overview
* Monitoring clinical studies in phases II-III.
* Assuring adherence to Good Clinical Practices, investigator integrity, and compliance with all study procedures.
* Identification, qualification and initiation of investigators and their sites.
* Supervising study conduct according to GCP requirements and all applicable laws.
Key Requirements
* Bachelor degree in life-science.
* Fluent English & Spanish.
* Excellent communication skills.
* A full clean drivers license.
* FTE: 1.0.
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