Clinical Research Associate I (CRA I) - São Paulo/SP
Core
Primary contact for assigned research sites throughout the clinical study lifecycle, ensuring compliance, data quality, and patient safety.
Role type
Junior Clinical Research Associate (CRA I)
Builds
Clinical trial sites across all phases of the study lifecycle
Domain
Healthcare / Clinical Research
Deliverable
physical/clinical work
Required skills
Clinical trial monitoring, Site management, Regulatory compliance (ICH-GCP), Data quality assurance, Protocol adherence, Documentation management, Cross-functional collaboration, Root cause analysis, CAPA implementation, Multicultural environment navigation
Preferred skills
Experience as Clinical Trial Assistant (CTA), Research Coordinator, or Research Nurse
Technologies
CTMS, eTMF, EDC, MS Office
Responsibilities
Conduct remote and on-site monitoring activities (qualification, initiation, monitoring, close-out), Review and maintain study and regulatory documentation, Support site activation and achieve Site Ready status, Identify and escalate site performance or compliance issues, Maintain accurate documentation in clinical systems, Support audit and inspection activities
Seniority
Junior, hands-on IC