Company Description
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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 Madrid
Experience in commercial studies
Experience with site initiation, site close out
Experience xpzdshu in clinical studies phase II-III
Fluent English & Spanish
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 or email .uk
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