Clinical Research Study Activations Coord

The Study Activations Project Coordinator is responsible for coordinating initial study start-up and submission activities, including the coordination of Research Review Committee, Feasibility Committee, and Accrual sub-committee.

Requirements

• 5 years experience with computer programs particularly Microsoft Suites or related
• 1 year experience with project coordination/or involvement with implementing projects
• 1 year experience coordinating Clinical Trial Management System activities
• 1 year experience in clinical research
• 2 years experience in research or healthcare related office setting preferably oncology or clinical trials

Benefits

• Generous Paid Time Off
• 401k Matching
• Retirement Plan
• Equal Opportunity Employer/Veterans/Disabled