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.
IQVIA provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
