CRA pharma Rotterdam
Full Time
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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 / Clinical Research Associate sponsor dedicated in Rotterdam.
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 1 year monitoring experience as CRA within a CRO, Pharma, Biotech in Netherlands
- Experience in commercial studies
- Experience with site initiation, site close out
- Experience in clinical studies phase II-III
- Fluent English & Dutch
- Excellent communication skills
- A full clean drivers license
- FTE: 1.0
If you have difficulty in applying, have any questions or you cannot find what you are looking for please contact us on 0044 (0) 207 421 0000 or email [email protected]
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