CRA 2, Oncology, IQVIA

IQVIA seeks a Clinical Research Associate 2 for oncology studies with 1.5+ years of on-site monitoring experience. The role involves conducting site monitoring visits, managing recruitment, ensuring protocol compliance, and maintaining regulatory documentation across multiple locations.

Responsibilities

• Conduct site selection, initiation, monitoring, and close-out visits per protocol and regulatory standards
• Partner with sites to develop and track subject recruitment plans
• Administer protocol training and establish ongoing communication with study sites
• Review site practices for protocol adherence and regulatory compliance; escalate quality issues
• Track study progress including approvals, enrollment, CRF completion, and data queries

Requirements

• Bachelor's degree, preferably in scientific or healthcare discipline
• 1.5 to 2 years of CRA experience including on-site monitoring
• Knowledge of Good Clinical Practice (GCP) and ICH guidelines
• Experience with protocol training and site management
• Proficiency in clinical trial documentation and regulatory requirements
• Oncology study experience

Compensation: $90,200–$150,400 base