Responsible for the implementation, management and oversight of research studies, including educating research staff, healthcare team members, participants, and caregivers. Registers, compiles, submits, and oversees clinical data; monitors study compliance; and maintains an effective system for data flow for patients on clinical trials. Manages patient visits and implements protocol-related procedures. Monitors and communicates study participant progress and safety issues with investigators, applicable regulatory agencies, the healthcare team, and study staff.
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Job Type
Full-time
Education Level
No Education Listed