Texas Licensed Senior CRA

Job Summary

Focusing on oncology studies, the full-time Senior Clinical Research Associate, Texas Licensed CRA, will conduct independent monitoring visits, manage site relationships, and ensure compliance across clinical trials primarily in Texas.

Key responsibilities

• Conduct all monitoring visits from initiation through close-out independently
• Manage site relationships to ensure compliance, enrollment, and protocol adherence
• Identify risks and implement corrective/preventive actions (CAPAs) while reviewing CRFs and resolving data queries

Required qualifications

• 5+ years of independent CRA monitoring experience
• 2+ years of oncology monitoring experience preferred
• Strong knowledge of ICH-GCP and regulatory requirements