Sr. CRA I (Sponsor dedicated) - Sao Paulo, Brazil Home Based

Senior Clinical Research Associate dedicated to sponsor activities; responsible for site qualifications, monitoring, and close‑out visits in both on‑site and remote settings.

Job Responsibilities

• Perform site qualification, site initiation, interim monitoring, site management and close‑out visits in compliance with regulatory, ICH‑GCP, and Good Pharmacoepidemiology Practice guidelines; evaluate site performance and provide recommendations.
• Verify informed consent procedures and document safety and data integrity issues at investigator sites.
• Conduct source document reviews, verify CRF data accuracy and completeness, and resolve queries within agreed timelines.
• Manage investigational product inventory, reconciliation, dispensing, and storage; ensure proper labeling, import, release, or return of IP.
• Review Investigator Site Files for accuracy and r...