Senior Clinical Research Associate I — Sponsor‑Dedicated

Syneos Health, Inc.; España; Sur place; EUR 60 000 - 85 000; Plein temps

Résumé du poste

Syneos Health in Madrid, Spain, seeks a Sr CRA I / Sr CRA II for sponsor-dedicated monitoring. You will perform site qualification, initiation, interim monitoring, site management and close-out visits on-site or remotely, ensuring regulatory and ICH-GCP compliance.

You will assess site performance, verify informed consent, review source documents and CRFs, resolve queries, manage ISF/TMF, and support subject recruitment and data integrity, while adapting to changing priorities to meet project

Responsabilités

• Site qualification, initiation, interim monitoring, site management and close-out visits (on-site or remote).
• Ensure regulatory, ICH-GCP and GPP protocol compliance and escalate issues to the project team.
• Verify informed consent processes and protect patient confidentiality.
• Review source documents and CRFs for accuracy and completeness; apply query resolution.
• Maintain ISF/TMF alignment and support data capture and tracking of observations.

Description du poste

Syneos Health in Madrid, Spain, seeks a Sr CRA I / Sr CRA II for sponsor-dedicated monitoring. You will perform site qualification, initiation, interim monitoring, site management and close-out visits on-site or remotely, ensuring regulatory and ICH-GCP compliance.

You will assess site performance, verify informed consent, review source documents and CRFs, resolve queries, manage ISF/TMF, and support subject recruitment and data integrity, while adapting to changing priorities to meet project