layiq

/la·yiq/adjective

worthy; deserving; fitting; suitable.

A role, opportunity, or path that merits attention, time, and pursuit.

LAYIQ - Clinical Research Coordinator Associate at Stanford University

Coordinate study activities from startup through close-out, including participant recruitment, screening, scheduling, enrollment, data collection, and follow-up.
Serve as a primary contact for research participants, families, sponsors, regulatory agencies, and community partners.
Communicate regularly with prospective and enrolled families in a professional, supportive, and culturally appropriate manner.
Determine participant eligibility, obtain informed consent according to protocol, and assist with recruitment and community outreach strategies.
Serve as a primary data collector for child and parent assessments, including administering surveys, questionnaires, and standardized interview questions.
Explain study procedures to participants in a clear, professional, and participant-friendly manner.
Collect child and parent study data according to standardized research protocols, study manuals, and certification requirements.
Conduct anthropometric and related body composition measurements, including height, weight, waist circumference, and other study-specified measures.
Coordinate and administer health behavior assessments, including physical activity, sedentary behavior, sleep, screen time, and dietary assessment procedures.
Enter, manage, and track participant data in secure study databases accurately and promptly.
Develop and maintain study-related documents, flow sheets, case report forms, tracking logs, and other study materials.
Review study records and case report forms for completeness and accuracy against source documents.
Track assessment completion, coordinate reminders and make-up visits, and proactively follow up with families to minimize missing data.
Ensure compliance with research protocols, institutional requirements, IRB approvals, and regulatory documentation standards.
Prepare regulatory submissions and assist with IRB renewals, monitor visits, sponsor meetings, and regulatory audits.
Interact regularly with the principal investigator and study team to ensure participant safety, data quality, and adherence to proper study conduct.
Assist with training and supervision of additional study staff related to recruitment, enrollment, assessment procedures, and data collection.
Participate in delivery of weekly group health behavior change sessions for children and parents during evening hours.
Participate in family engagement and participation throughout the intervention program.
- Other activities as needed to assist in the successful conduct of the study.

Clinical Research Coordinator Associate

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