Cra Madrid – Regional Monitoring

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 Regional Monitoring in Madrid.
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 and site close out.
Experience in clinical studies phase II-III.
Fluent in English Spanish.
Excellent communication skills.
A full clean drivers license.
FTE: 1.0.
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