CRA 2, Oncology, IQVIA
$90.2k - $150.4kIQVIA
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
Vacancy posted 14 days ago
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