Senior Clinical Research Associate — Hybrid Trial Monitoring
CTI Clinical Trial and Consulting Services
CTI Clinical Trial and Consulting Services is seeking a Clinical Trial Monitor to act as the primary CTI contact for assigned study sites across monitoring activities. You will conduct PSV, SIV, IMV, and COV visits, ensure regulatory compliance, and support start-up activities, site selection, and data/document tracking. The role involves working with regulatory affairs, project teams, and site staff to ensure high-quality study execution and timely deliverables. #J-18808-Ljbffr CTI Clinical Trial and Consulting Services
Vacancy posted 2 days ago
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