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
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