OPIS s.r.l.
Clinical Research Associate
- Tiempo completo
- Gestion de proyectos
- Biomedicina
50000 €/año
... investigational sites - Conduct feasibility, pre-study, initiation, monitoring, and close-out visits - Ensure compliance with protocols, SOPs, ICH-GCP, and regulatory requirements - Perform source data verification and ensure data accuracy and completeness - Monitor patient recruitment and support sites in meeting targets ...
Barcelona, España