What are the responsibilities and job description for the Clinical Trial Systems Coordinator - 236244 position at Medix?
Systems Coordinator - Job Description
Support the ongoing maintenance activities for the CTO Clinical Research Management System (CRMS). Facilitate regulatory review process by providing customer support and assist in training of Clinical Research Systems users. Perform Quality Control and Quality assurance activities to verify and maintain accurate and complete protocol metadata in Clinical Research Systems. Provide metric reporting and study tracking as required by Senior Leadership.
Acts as a resource for day to day issues (elbow support) and providing support to staff; and also supports Management and Leadership on projects and initiatives. Facilitate regulatory review process by providing customer support and assist in training of Clinical Research Systems users. Perform Quality Control and Quality assurance activities to verify and maintain accurate and complete protocol metadata in Clinical Research Systems. Provide metric reporting and study tracking as required by Senior Leadership.
Schedule / Shift
Mon-Fri : 8-5
5 days onsite during probationary period (90 Days)
3 days onsite after, 2 remote days
