CRA II, Multisponsor ** Hybrid MADRID or BARCELONA **

Experteer Overview
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In this role you support clinical trials as a CRA II, guiding site qualification, monitoring, and close-out to ensure regulatory and protocol compliance. You work with cross-functional teams to manage site performance, data integrity, and safety considerations, both on-site and remotely. You contribute to audit readiness and investigator interactions while advancing real-world late-phase study goals. You join a collaborative environment focused on delivering high-quality trials and shaping patient outcomes.
Compensaciones / Beneficios
• Perform site qualification, initiation, monitoring, and close-out visits (on-site or remote) ensuring ICH-GCP/GPP compliance.
• Evaluate site performance and escalate issues with action plans to project teams.
• Verify informed consent process, protect subject confidentiality,...