
This full-time Clinical Trial Coordinator II role supports the planning and execution of global clinical studies within a fast-paced pharmaceutical environment. The position involves reviewing essential study documentation, overseeing risk-based monitoring, and ensuring regulatory inspection readiness in collaboration with study teams and external vendors. The role offers the opportunity to work on high-complexity Phase 2 and 3 trials across multiple therapeutic areas while developing expertise in international compliance standards. The position is based in an office setting with standard business hours, providing a collaborative atmosphere for professionals seeking to advance their careers in clinical research operations.













