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 in Netherlands. The role is sponsor dedicated via the CRO
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
Min 3 monitoring experience as CRA / Clinical Research Associate within a CRO, Pharma, Biotech
Experience in commercial studies
Experience with site initiation, site close out
Experience in clinical studies phase II-III
Fluent Dutch English
Excellent communication skills
A full clean drivers license
FTE: 1.0
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