Job Overview:
Supports and coordinates clinical research studies within the Radiology department. Ensures protocol compliance, manages study activities, and serves as a key liaison between internal teams, investigators, and external partners.
Key Responsibilities:
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Coordinate and manage MRI/radiology-related clinical research projects
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Serve as liaison between investigators, IRB, sponsors, and internal departments
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Track study participants in accordance with protocols
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Maintain accurate study documentation, regulatory files, and adverse event reporting
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Assist with scheduling and coordination of research-related procedures
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Monitor and ensure compliance with study requirements and data integrity
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Collaborate with cross-functional teams (e.g., oncology, transplant, neuroscience) on research initiatives
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Support staff training and onboarding related to research protocols and procedures
Requirements:
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Bachelor’s degree or relevant experience in clinical research or healthcare field
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Minimum 2 years of clinical research or healthcare coordination experience
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Knowledge of clinical trial processes, regulatory requirements, and documentation practices
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Experience working with IRB processes and human subject research preferred
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Strong organizational, communication, and coordination skills
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Ability to manage multiple projects and stakeholders