Clinical Research Associate: Site Monitoring

IQVIA is seeking a Clinical Research Associate to perform site monitoring visits and ensure studies are conducted per protocol and regulations. You will manage site communications, training, and documentation.You will track recruitment, CRF completion, data queries, and regulatory submissions, and support start-up and TMF/ISF maintenance. Strong English and...

IQVIA LLC is seeking a Clinical Research Associate to monitor study sites and ensure data reported aligns with protocol and regulatory requirements. You will manage site communications, train staff, and track regulatory submissions, recruitment, and data queries.Milano-based, onsite role requiring strong English communication and organized project oversight....

IQVIA LLC in Milano, Italy, is seeking a Clinical Research Associate to monitor sites and manage studies, ensuring protocol adherence and data quality.You will conduct monitoring visits, coordinate with site staff, and support regulatory compliance across assigned sites in Italy, applying solid GCP/ICH knowledge and strong English communication.This role...

IQVIA LLC in Milano, Italy, is seeking a Clinical Research Associate to monitor sites and manage studies, ensuring protocol adherence and data quality.You will conduct monitoring visits, coordinate with site staff, and support regulatory compliance across assigned sites in Italy, applying solid GCP/ICH knowledge and strong English communication.This role...

Oxford Global Resources is seeking a Clinical Affairs support professional to help ensure study site selection and conduct in compliance with GCP and federal regulations. The role involves on-site monitoring activities and coordination of supplies across study sites, working with the Clinical Affairs team. The candidate should have 2+ years in clinical...

BeOne Medicines in Milano, Italy seeks an experienced Clinical Research Associate to monitor oncology trials across sites, ensuring adherence to ICH-GCP, local regs, and BeOne SOPs. You will perform feasibility and site identification, initiate and conduct visits, and support data quality and timely milestones.The role requires a BS in a scientific...

IQVIA is seeking a Clinical Research Associate to perform site monitoring visits and ensure studies are conducted per protocol and regulations. You will manage site communications, training, and documentation. You will track recruitment, CRF completion, data queries, and regulatory submissions, and support start-up and TMF/ISF maintenance. Strong English...

IQVIA LLC is seeking a Clinical Research Associate to monitor study sites and ensure data reported aligns with protocol and regulatory requirements. You will manage site communications, train staff, and track regulatory submissions, recruitment, and data queries. Milano-based, onsite role requiring strong English communication and organized project...

h3Job Overview /h3pPerform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. /ph3Essential Functions /h3ulliPerform site monitoring visits (selection, initiation, monitoring and close‑out visits)...