Clinical Research Associate: Site Monitoring

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...

pICON Clinical Plc in Lombardia, Italy is seeking a CRA II to design and analyze clinical trials, monitor sites, collaborate with investigators, and contribute to study documentation.You will help uphold data integrity and patient safety while advancing innovative therapies./ppThe role supports cross-functional teams in a fast-paced, global environment,...

ICON Clinical Plc in Lombardia, Italy is seeking a CRA II to design and analyze clinical trials, monitor sites, collaborate with investigators, and contribute to study documentation. You will help uphold data integrity and patient safety while advancing innovative therapies.The role supports cross-functional teams in a fast-paced, global environment,...

Overview In this role you support multicenter clinical studies by monitoring sites to ensure protocol adherence and data reporting per GCP/ICH guidelines. You will drive site communication, training, and recruitment alignment to project needs, and manage study progress and documentation in collaboration with the study team. The role includes ensuring TMF/ISF...

Overview In this CRA role at Medpace you will support the integrity of clinical studies across pharmaceutical and medical device development. You’ll join a training-focused program (PACE) that accelerates your skills toward independent CRA responsibilities. You work across sites, regulators, and cross-functional teams to ensure compliant trials and data...

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer. General Description: * The CRA executes clinical...

Provide support to Clinical Affairs team to assure study site selection and conduct of the study by study sites in compliance with Good Clinical Practices, federal regulations, and Clinical Affairs SOPs through in-house and some on-site monitoringConduct pre-study visits to assure the site has adequate facilities, staff, and subject population for conducting...

SummarySede: Field Force ItaliaSupporto alla Relocation: Questa posizione ha sede in Italia.Novartis non è in grado di offrire supporto per il trasferimento; ti invitiamo pertanto a candidarti solo se la sede è facilmente raggiungibile per te.Entra in un ruolo in cui il tuo lavoro contribuirà direttamente al progresso dell'innovazione clinica e ad...

As a CRA II at ICON, you design and analyze clinical trials, ensuring data integrity and patient safety while advancing innovative therapies. You will monitor sites, collaborate with investigators, and contribute to study documentation. This role supports cross-functional teams in a fast-paced, global environment and involves travel. You will help bring new...