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 2 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
Please email your to [email protected].