Lead clinical trial delivery for ICON, overseeing study start-up, execution, compliance, risk management, budgets, and closeout. Partner with sponsors and study teams to deliver high-quality research programs.
Monitor sponsor-dedicated clinical trials for ICON, a global clinical research organization. Support protocol compliance, reliable data, and patient safety across Canadian trial sites.
Monitor sponsor-dedicated clinical trial sites for ICON Strategic Solutions while supporting regulatory compliance, patient safety, data quality, and site performance. This role serves as a key link between study sponsors and investigational sites.
Lead end-to-end clinical trial delivery for ICON plc, including study oversight, enrollment, budgets, start-up, and regulatory compliance. Guide cross-functional teams and support successful outcomes across complex clinical research programs.
Senior Clinical Research Associate supporting sponsor-dedicated oncology trials for ICON plc. The role oversees site monitoring, regulatory compliance, data quality, and resolution of clinical trial issues.
Monitor respiratory and cardiovascular clinical trials for ICON Strategic Solutions across Canada's Greater Toronto Area. Coordinate site visits, compliance, data quality, and guidance for clinical research teams.
Monitor cardiovascular and respiratory clinical trials across Quebec for ICON plc, supporting site compliance, data quality, and adherence to study protocols.
ICON plc is hiring a remote Senior Clinical Research Associate in Brazil to monitor clinical trial sites, uphold ICH-GCP and protocol standards, and support accurate, compliant study execution.
Support clinical trial administration and operational delivery for ICON’s sponsor-dedicated pharmaceutical services. Coordinate regulatory documentation, site communications, trial records, and stakeholder activities.
ICON plc is seeking a Senior Clinical Research Associate to monitor respiratory and cardiovascular trials across the Greater Toronto Area. The role oversees site performance, regulatory compliance, data quality, and trial delivery.
Monitor respiratory and cardiovascular clinical trials for ICON across the Greater Toronto Area. Support GCP compliance through site oversight, study visits, data integrity, and stakeholder guidance.
Lead remote monitoring for Phase I oncology trials with ICON Strategic Solutions. Oversee sites, compliance, data quality, and CRA support.
Monitor clinical trials for ICON’s sponsor-dedicated research programs across Canadian sites. Support protocol adherence, reliable data, and patient safety throughout each study.
Monitor respiratory and cardiovascular clinical trials for ICON’s sponsor-dedicated research operations. Oversee GTA sites, compliance, data quality, and trial delivery.
संयुक्त राज्य
कैलिफ़ोर्नियाLead Phase I oncology trial monitoring for ICON’s sponsor-dedicated research programs. Oversee sites, compliance, data integrity, and clinical research associate guidance.
Lead clinical trial monitoring, site oversight, and compliance activities for ICON’s sponsor-dedicated research programs in Malaysia.
Lead sponsor-dedicated clinical trials for ICON plc in Malaysia, coordinating operations, stakeholders, compliance, risk, and delivery quality. This full-time remote role supports clinical programmes from planning through execution.
Clinical Research Associate II responsible for monitoring clinical trials remotely from Malaysia, maintaining protocol compliance, data quality, and participant safety across study sites for ICON.
संयुक्त राज्य
एरिज़ोनाकैलिफ़ोर्निया
कोलोराडो
यूटाICON plc is hiring a Senior Clinical Research Associate to monitor sponsor-dedicated Phase I oncology trials remotely from the United States. The role oversees sites, maintains GCP compliance, and supports clinical trial teams.
Lead clinical data management teams supporting ICON’s sponsor-dedicated research services. Oversee people, delivery, quality, compliance, client relationships, resources, and operational improvement.
