Medpace, Inc.
Location
Denver, Colorado
The role involves engaging in day-to-day clinical trial management, working closely with the CTM to ensure timely and accurate task delivery. Responsibilities also include compiling status reports, interacting with various stakeholders, and managing internal regulatory filing oversight and study supplies.
Candidates must possess a Bachelor's degree in a health or life sciences field and should have prior experience as a Study Coordinator or within the pharmaceutical industry. Excellent skills in computer applications, organization, and communication are also required.
Engage in clinical trial management on a day to day level; Work closely with the project CTM for timely delivery of tasks consistently with a high degree of accuracy; Compile and maintain project-specific status reports; Interact with the Sponsor, study sites, and internal associates; Provide oversight and quality control of our internal regulatory filing system; Manage study supplies; Create and maintain project timelines; and Coordinate project meetings and produce quality meeting minutes.
Why Medpace?
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