Supervisor, Clinical Coordination (Normal,IL) - (Normal, IL)

Purpose: Manage the day-to-day Coordination activities within Clinical Supply Management (CSM). The main objective of this function is to convert the manufacturing requests into executable Batch Records for the Packaging Line. Primary responsibilities: Responsible for compliance with applicable policies and procedures. Accountable for compliance with global GMP and regulatory regulations and qualifications in own area. Manage and supervise staff to ensure that all clinical studies start on time with no patient dosing interruptions. Coordinate pre-packaging and post-packaging activities including the generation of packaging instructions. Work with the Scheduling, Packaging and QA groups to coordinate the packaging schedule and batch record reviews to ensure all timelines are met. Develop tools to collect baseline and ongoing key performance metrics that measure and monitor the productivity and efficiency of the Clinical Coordination group.