Clinical Research Associate: Site Monitoring & Data Quality
IQVIA
IQVIA is seeking a Clinical Research Associate to perform on-site monitoring visits in accordance with GCP and protocol requirements. You will ensure site readiness, oversee data quality, and engage with sites to support recruitment and regulatory submissions.
The role requires at least 2 years of independent CRA experience, strong regulatory knowledge, and excellent communication. Proficiency with EDC/CTMS/eTMF is expected.
#J-18808-LjbffrVacancy posted 4 days ago
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