Senior Clinical Research Associate

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 Travel 2-3 days per week Min 2 year monitoring experience as CRA within a CRO, Pharma, Biotech Experience in commercial studies Experience with site initiation, site close out Experience in clinical studies phase II-III Fluent English & Italian Excellent communication skills A full clean drivers license FTE: 1.0 Please feel free to email your cv at [email protected]