LEAD SYSTEM COORDINATOR - CLINICAL TRIALS OFFICE
About The Position
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.
Requirements
- Bachelor's Degree in Computer Science, Information Systems, or related field Required
- Combination of relevant education and experience may be considered in lieu of degree Required
- 5 years experience working with Clinical Research Software Required
Nice To Haves
- Master's Degree Computer Science, Information Technology, or Science related field Preferred
- 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
- Clinical Research Management Preferred
Responsibilities
- 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
- 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.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Industry
Hospitals
Number of Employees
1,001-5,000 employees
