Specific responsibilities and key duties involve screening, recruitment, scheduling and retention of study participants, collection of psychological, behavioral, biological and clinical data at study visits, abstraction of data from medical records, management of research databases, isolation and culture of stem cells from newborn blood and tissues, processing and storage of biospecimens (e.g., blood, saliva, urine), conducting infant non-invasive scans/phenotyping (e.g., skinfold, anthropometric measurements, PeaPod, magnetic resonance imaging scans (MRI)), and management and ordering of research supplies for the clinical and laboratory spaces. Accordingly, the Clinical Research Coordinator is responsible for the day-to-day implementation, coordination, and oversight of human subjects study activities, including participant screening, recruitment and retention, informed consent, study visits, data management, regulatory compliance, and study logistics, and is additionally responsible for laboratory management including biospecimen collection and processing, and laboratory supply and equipment management.