Clinical Research Associate: Site Monitoring

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....

ICON is seeking a Clinical Research Associate to contribute to the design and analysis of clinical trials within sponsor-dedicated model. You will monitor sites, ensure protocol adherence, data integrity, and patient safety, and collaborate with investigators to ensure smooth study conduct.You will review data, resolve queries, and help prepare study...

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....

ICON is seeking a Clinical Research Associate to contribute to the design and analysis of clinical trials within sponsor-dedicated model. You will monitor sites, ensure protocol adherence, data integrity, and patient safety, and collaborate with investigators to ensure smooth study conduct.You will review data, resolve queries, and help prepare study...

ICON is seeking a Clinical Research Associate to contribute to the design and analysis of clinical trials within sponsor-dedicated model. You will monitor sites, ensure protocol adherence, data integrity, and patient safety, and collaborate with investigators to ensure smooth study conduct.You will review data, resolve queries, and help prepare study...

Job OverviewPerform 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.La preghiamo di leggere attentamente le informazioni contenute in questo annuncio di lavoro per comprendere esattamente cosa ci...

Clinical Research Associate/Senior Clinical Research Associate/CRAVerifichi qui sotto se possiede i requisiti per questa opportunità e, in tal caso, invii la sua candidatura il prima possibile.ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.As a...

In this role, you contribute to the design and analysis of clinical trials within ICON's sponsor-dedicated model. You will monitor sites, ensure protocol adherence, data integrity, and patient safety, and collaborate with investigators to ensure smooth study conduct. You'll review data, resolve queries, and help prepare study documents to support trial...

General Description:The CRA executes clinical monitoring activities at clinical trial sites and monitors clinical trials in accordance with ICH guidelines and GCP, local regulations, and applicable SOPs. Performs monitoring activities related to selection, initiation, conduct (recruitment, quality data collection) and timely completion of oncology/hematology...