CRA 2, Oncology, IQVIA
IQVIA · Durham, NC +15 more
Clinical OperationsFull-time$87k–$145kCompany career page
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Role summary
IQVIA is hiring a Clinical Research Associate 2 for oncology studies across multiple U.S. locations. The role involves conducting site monitoring visits, managing study progress, ensuring regulatory compliance, and coordinating with clinical trial sites to support protocol execution and data integrity.
What they're looking for
- Bachelor's degree in scientific discipline or healthcare field
- 1.5 to 2 years of clinical research associate experience
- Minimum 1.5 years of on-site oncology monitoring experience
- Knowledge of Good Clinical Practice (GCP) and ICH guidelines
- Experience with case report form management and data queries
What you'll be doing
- Conduct site monitoring visits including selection, initiation, monitoring, and closeout phases
- Manage subject recruitment planning and track enrollment progress with assigned sites
- Administer protocol training and maintain communication with study sites
- Evaluate site compliance with protocol requirements and applicable regulations
- Prepare monitoring visit reports, follow-up documentation, and maintain Trial Master Files
Key requirements
- Therapeutic area
- Oncology
Privacy & handoff
This role links to IQVIA's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.