Role Description
This is a contract role for a Clinical Research Coordinator, located on-site in Bryn Mawr, Pennsylvania. The Clinical Research Coordinator will be responsible for managing the day-to-day clinical trial activities, obtaining informed consent from study participants, ensuring protocol adherence, conducting clinical research tasks, and managing clinical trial documentation.
Qualifications
NOTE: This role will start at 20 hrs/week with ability to convert to full-time.
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