Role OverviewProvides daily departmental administrative guidance and reports for conduct of new research and new sponsored projects, coordinates clinical research studies, and ensures hospital and Institutional Review Board (IRB) approval for research studies.
What You Will Do
Coordinates activities associated with site start-up, develops and maintains processing and tracking systems for protocol related paperwork, and prepares and submits various reports to sponsors, investigators, and regulatory authorities.
Why It Might Be a Fit
Collaborative work with all departments to provide support for clinical trials goals, requires independent working knowledge of Clinical trial management system, electronic health record, spreadsheet and database software.
Requirements
- Bachelor’s Degree in Administration, Business, or Related Field
- 3 years experience in research administration, clinical research, or project management
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