Clinical Trails Monitor II
Core
Develops and manages study-specific strategies to ensure clinical trial kits are available when and where needed while minimizing inventory and waste.
Role type
Senior IC clinical trial supply monitor
Builds
Study-specific start-up and resupply strategies for clinical trial kits
Domain
Clinical research operations / Clinical trial supply chain
Required skills
Clinical trial protocol analysis, Study feasibility assessment, Supply strategy design, System configuration, Quality control, Active study monitoring, Exception management, Performance analysis, Training delivery, Cross-functional coordination
Preferred skills
Clinical trial kit supply experience, Central laboratory services knowledge, Therapeutic area/patient pathway understanding, Rule-based operational services experience, Client meeting facilitation
Technologies
Labcorp Smart Supply systems, Dashboards, Trackers, Source data systems
Responsibilities
Review clinical trial protocols and documentation to determine service scope; Lead discussions with clients on supply strategy and risks; Develop start-up and resupply strategies based on enrollment and site activity; Configure and maintain internal supply systems; Monitor study activity and adjust strategies as conditions change; Investigate system exceptions and coordinate corrective actions; Analyze performance data to identify waste and risks; Provide training and maintain study documentation.
Seniority
Mid-Senior, hands-on IC
