This individual will provide mid-level research support as a Project Coordinator. The position is part of the Management Core for a network of clinical trials and focuses on support for the communication with personnel at the Management Core, clinical sites, and the funding agency. Duties include coordinating site sub-awards and reimbursements, assisting with site monitoring (reports, status updates), organizing and attending study meetings and conference calls, tracking regulatory and other project-related documentation, writing and editing manuals, preparing reports and assisting with IRB submissions.
Executes protocol-related research procedures, activities, outreach, and education. Manages a complex program or study or multiple programs and studies. Collects and analyzes data and complies with all policies and regulations. Recommends improvements to policy and procedure.
Work is expected to be done autonomously with overall guidance and direction from leadership.
Ability to follows prescribed procedures.
Routine problem solving is required, generally guided by policies, procedures and business plans.
Little physical effort required. Duties are primarily sedentary. May be required to move objects up to 25 pounds occasionally.
PI287633414