Description
The Clinical Research Coordinator will coordinate and oversee the daily operations of clinical trials, including patient recruitment, informed consent, visit scheduling, data collection, documentation, regulatory compliance, and adverse-event reporting. The role serves as a liaison among investigators, study sponsors, and English- and Spanish-speaking participants, with a focus on psychiatric and behavioral health studies. Required qualifications include a bachelor’s degree in a health-related field, at least two years of clinical research coordination experience, bilingual English-Spanish proficiency, and knowledge of clinical trial processes and regulatory requirements.
