CRA II_Barcelona_Sponsor dedicated. Experience in onco-hematology, and gynecologic oncology clinical
Hace 4 días
Zaragoza, Zaragoza (comarca); Provincia de Zaragoza; Aragón, España
Syneos Health
Jornada completa
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Overview In this CRA II role, you will oversee clinical trial activities to ensure protocol and regulatory compliance across sites. You will work closely with site teams and cross-functional partners to monitor data integrity, patient safety, and trial progress. You’ll apply risk-based monitoring techniques and drive site performance improvements to support study success. This is a mission-driven opportunity to help accelerate healthcare progress through rigorous trial oversight.
technical and therapeutic area training
Conduct site qualification, initiation, monitoring, and close-out visits (on-site or remote) ensuring ICH-GCP/GPP compliance
Assess site performance and provide actionable recommendations; Verify data quality and source document integrity; perform IP inventory and handling per protocol
Review ISF and TMF reconciliation; Coordinate training and communication with site staff; adapt to project scope, budgets, and timelines
May train junior staff and identify out-of-scope activities for escalation
Bachelor in related field
Experience in oncology, hematology, and gynecologic oncology clinical trials
electronic data capture (EDC) systems usage