Job Summary
IQVIA is looking for a proficient Clinical Research Associate specializing in sponsor-dedicated monitoring and site management throughout various regions in the United States. This position requires significant experience within clinical sites, focusing on ensuring compliance and facilitating successful study outcomes.
Responsibilities
- Conduct site monitoring visits to ensure adherence to protocol, regulatory requirements, and sponsor expectations.
- Evaluate site performance and manage communication with study personnel to address issues proactively.
- Support the recruitment and retention strategies for study participants.
- Maintain accurate records of site activities and monitor site compliance with study protocols.
Qualifications
- Bachelor’s degree in life sciences or nursing (U.S. equivalent or higher).
- Prior experience in a clinical research setting, particularly with site level monitoring.
- Strong understanding of clinical research processes and regulatory compliance.
- Excellent communication and organizational skills.
