Location
Irvine
Job Type
Full-time
Posted
June 16, 2026
Job Description
On Site Role
Hours: Mon-Fri, 8am - 5pm
Job Description:
Identify, develop, recommend, and implement, moderately complex process development and process improvement solutions to optimize global trial workflow timelines, (e.G., device return aging issues, status of open device issues/queries, etc.)
Develop and execute device processes associated with clinical trials.
Ensure compliance with regulations and manage the lifecycle of devices, while closely partnering with other internal key stakeholders ( e.G., clinical study teams, Manufacturing Operations, Finance, Supply Chain, Quality, and Compliance groups) to develop and lead the execution of the device process, and ensuring continuous process improvement of efficiency and accuracy of processes and procedures.
Verify inventory and process device shipment to clinical sites within our shipping timeframe to Customer Service, Trade Compliance, and other rele...