Coordinates and assists with the implementation of multiple clinical research studies. Responsible for training and educating staff. Coordinates the preparation and delivery of departmental communications, presentations and marketing/educational materials. Collaborates to ensure the compliance with local, state and federal regulations and standards. Assists with responding to and preparing for audits and participates in audits. Processes and ships research specimens per protocol guidelines. Manages the handling of adverse events, compliance and other participant-related issues. Handles resolution of data queries with sponsor. Responsible for completing, organizing, and submitting Institutional Review Board (IRB) for phase 1 - 4 trials required by the sponsor. Conducts initiation, monitoring and close out visits with the sponsor. Assists in training/mentoring of CRC I and other team members as required.
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Job Type
Full-time
Career Level
Mid Level
Education Level
High school or GED