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 Andalusia.
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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