Medpace is seeking a full-time, Global Study Start-Up Project Manager to join their Clinical Operations team. This role is crucial to the clinical trial management process and involves managing the successful execution of global start-up, maintenance, and close-out studies. The position requires leading others in a matrix environment, performing quality checks on submission and site essential documents, preparing and approving informed consent forms, and serving as a Sponsor point of contact for start-up and regulatory submissions. The role also involves reviewing regulations to develop proactive solutions, preparing new business proposals, and contributing to departmental growth.
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Job Type
Full-time
Career Level
Senior