This role is responsible for driving research protocol execution by collaborating with principal investigators, sponsors, and clinical teams to plan, conduct, and evaluate study initiatives. The position also involves leading participant engagement strategies to recruit, schedule, and monitor clinical trial subjects while maintaining safety and patient-centric care. The coordinator will oversee compliance and adverse event protocols, manage Institutional Review Board (IRB) communications, and deliver clear departmental messaging through educational materials and presentations.
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Job Type
Full-time
Career Level
Mid Level
Education Level
High school or GED