LEAD SYSTEM COORDINATOR - CLINICAL TRIALS OFFICE

Advance the ongoing maintenance activities for the CTO Clinical Research Management System (CRMS). Oversees and supervises the System Coordinators in the overall operations, training and oversight of the team. Acts as a resource for day to day issues and providing support to staff; and also supports Management and Leadership on projects and initiatives. Provides oversight and guidance on team-member workloads and assignments. 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.

Education
Bachelor's Degree in Computer Science, Information Systems, or related field Required
Master's Degree Computer Science, Information Technology, or Science related field Preferred or
Combination of relevant education and experience may be considered in lieu of degree Required

Experience
5 years experience working with Clinical Research Software Required
5 years experience working in Clinical Research Operations and Coordination Preferred
General Experience and knowledge of database applications and theory, clinical research software systems, medical research methods and operations, medical terminology and computer report generation software; and financial, HR, EHR, and Grants Systems Design and Implementation Preferred

Licenses
Clinical Research Management Preferred