Under administrative review, performs management level work directed toward the planning, development, implementation, and evaluation of the assigned project(s). Requires the use of judgment and discretion in performing the assigned duties and responsibilities related to the project. These actions tend to establish precedents and direction for the project. The role involves coordinating regulatory submissions, managing trial operations, adverse event reporting, patient reports, overseeing communications , supporting reporting workflows, and liaising with clinical research coordinators, data managers, and the Data Coordinating Center. Experience in clinical trial management, healthcare EMR systems (e.g., EPIC), and regulatory platforms is required.
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Job Type
Full-time
Career Level
Manager