- 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.
- Bachelor degree in life-science
- Min 1 year monitoring experience as CRA within a CRO, Pharma, Biotech in Spain
- 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
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Lead Clinical Research Associate - España - Resourcing Life Science
Descripción
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 Lead CRA / Clinical Research Associate in Spain
Job Overview
Key Requirements
If you have difficulty in applying, have any questions or you cannot find what you are looking for please contact us on or email -
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