The Clinical Trial Recruitment Specialist is responsible for ensuring volunteer participation for each clinical study. This role involves pre-screening potential participants, managing recruitment databases, scheduling screening appointments, and conducting telehealth procedures including informed consent, demographic collection, and medical history review. The specialist must maintain a thorough understanding of inclusion/exclusion criteria for active protocols and ensure strict adherence to Good Clinical Practices (GCPs). Collaboration with internal staff and community organizations is key to educating and recruiting participants. Quality assurance through data review is also a critical component of this role.
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Job Type
Full-time
Career Level
Entry Level
Education Level
Associate degree