Job Description
Can be fully remote
Job Posting Description
· Responsible for overall clinical study management, including planning, communication, coordination and practical tasks for the studies.
· Coordinates Ethical Committee and Institutional Review Board notifications.
· Creates, maintains and oversees study files and archiving.
· Manages testing laboratories including selection of laboratories for the studies.
· Manages clinical research organizations and ensures monitoring of studies, data collection and handling.
· Prepares, revises and maintains procedures for the conducting of clinical studies.
· Bachelor's or Master's Degree or equivalent.
· Post-graduate, certification, and/or license may be required.
· Typically, at least 3 - 5+ years relevant experience.
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