CRA Madrid – Regional Monitoring

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 in clinical studies phase II-III
• Fluent English & Spanish
• Excellent communication skills
• A full clean drivers license
• FTE: 1.0