Opportunity Description
Description
La siguiente información tiene como objetivo proporcionar a los posibles candidatos una mejor comprensión de los requisitos para este puesto.
CRA I, Multisponsor – Hybrid (Madrid or Barcelona)
Job Responsibilities
Perform site qualification, initiation, interim monitoring, site management activities and close‑out visits ensuring regulatory, ICH‑GCP and/or GPP compliance.
Verify informed consent process, protect patient confidentiality, and assess safety and data integrity issues.
Conduct source document review, verify CRF data accuracy and completeness, and resolve queries within agreed timelines.
Oversee investigational product inventory, reconciliation, dispensing, and compliance with local regulations.
Review Investigator Site Files, reconcile with Trial Master Files, and ensure archiving guidelines are met.
Document activities through letters, reports, and logs, and support recruitment, retention, and awareness strategies.
La siguiente información tiene como objetivo proporcionar a los posibles candidatos una mejor comprensión de los requisitos para este puesto.
CRA I, Multisponsor – Hybrid (Madrid or Barcelona)
Job Responsibilities
Perform site qualification, initiation, interim monitoring, site management activities and close‑out visits ensuring regulatory, ICH‑GCP and/or GPP compliance.
Verify informed consent process, protect patient confidentiality, and assess safety and data integrity issues.
Conduct source document review, verify CRF data accuracy and completeness, and resolve queries within agreed timelines.
Oversee investigational product inventory, reconciliation, dispensing, and compliance with local regulations.
Review Investigator Site Files, reconcile with Trial Master Files, and ensure archiving guidelines are met.
Document activities through letters, reports, and logs, and support recruitment, retention, and awareness strategies.
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