Performs basic nursing skills, study coordination, and data management, focusing on subject recruitment and enrollment, consistent study implementation, data integrity, and compliance with regulatory requirements and reporting. The role collects clinical information from participants, provides study education, obtains informed consent, and supports clinical-trial enrollment. It also coordinates communication, meetings, and progress tracking with consortium members and participating institutions. Additional duties may include collecting and processing specimen tissue, organizing research data, collaborating with the research team on goals and objectives, and supporting adherence to study protocols. The job description also includes extensive case-management, utilization-review, discharge-planning, and appeal-related duties, including applying medical-necessity criteria, documenting reviews, coordinating safe transitions of care, and referring cases to a Physician Advisor when needed.
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Job Type
Full-time
Career Level
Mid Level
Education Level
Associate degree