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Job Description
- Req#: 32748935515
Under the direction of the Senior Director, Clinical Trial Office Operations and the CTO leadership team with input from the Disease/ Modality (D/ M) Team Chairs and the Study Investigators, the Project Manager (PM), as a senior regulatory team member and leader, assists investigators with the submission and activation of their human subject research to the various regulatory committees who review and approve research including scientific review and IRB review. The CTO regulatory team facilitates a prompt submission of new protocols, study updates, amendments and other regulatory related materials to regulatory oversight committees by preparing committee applications and collecting documents for review. The PM serves as the primary point of contact for faculty, staff and sponsors for trial submission, approval and activation at COH. The PM is responsible for managing the initial study submission, ensuring proper D/ M Team endorsement and serves as the liaison to sponsor and submits res...Project Manager, Clinical Research, Manager, Research Coordinator, Operations, Clinical, HealthcareAbout the company
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