Clinical Research Associate 2, IQVIA
$74.5k - $197.5kIQVIA
IQVIA seeks a Clinical Research Associate II to conduct on-site monitoring for clinical trials across multiple therapeutic areas. The role involves site management, regulatory compliance, monitoring activities, and cross-functional collaboration to support study success.
Responsibilities
- Conduct site selection, initiation, routine monitoring, and closeout visits per regulatory requirements
- Build relationships with investigative sites and provide protocol and study-specific training
- Monitor study progress including site activation, patient recruitment, enrollment, and data quality
- Maintain study documentation, regulatory records, and Trial Master File compliance
- Prepare monitoring reports and support patient recruitment and retention efforts
Requirements
- Bachelor's degree
- Minimum 1 year independent on-site monitoring experience in CRO, biotech, or pharmaceutical
- Working knowledge of GCP, ICH, and clinical trial regulations
- Strong communication, organizational, and problem-solving skills
- Proficiency with Microsoft Office applications
Compensation: $74,500.00 - $197,500.00 base
Vacancy posted a month ago
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