CRA II, Multisponsor • Hybrid MADRID or BARCELONA

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Job Responsibilities

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• Performs site qualification, site initiation, interim monitoring, site management activities and close‑out visits (on‑site or remotely) ensuring regulatory, ICH‑GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance, and provides recommendations for site‑specific actions.
  
• Verifies informed consent procedures, protects confidentiality of subjects, and assesses factors that may affect safety and data integrity (e.g., protocol deviations, pharmacovigilance issues).
  
• Assesses site processes per the Clinical Monitoring/Site Management Plan, conducts source document review, verifies accurate and complete CRF data, resolves queries, and verifies electronic data capture compliance.
  
• Manages investigational produ...