Clinical Research Coordinator 2 (A)
Core
Mid-level clinical research professional assisting in planning, coordinating, implementing, monitoring, and evaluating specific clinical research studies from initiation to close-out.
Role type
Clinical Research Coordinator 2
Builds
Clinical research protocols in pulmonary, critical care, and sleep medicine
Domain
Healthcare / Clinical Research
Deliverable
physical/clinical work
Required skills
Participant recruitment and screening, Study procedures and data collection, Specimen collection and processing, Regulatory compliance (FDA/ICH-GCP), Adverse event reporting, Protocol amendment implementation, Data entry into EDC systems, Investigational product handling
Preferred skills
Phlebotomy certification, Experience with pulmonary function testing, Knowledge of sleep disorder studies
Technologies
EDC systems (Medidata, REDCap), Office software
Responsibilities
Assist in participant recruitment, retention, and eligibility screening; Perform study procedures and routine tests; Collect, process, pack, and ship biological specimens; Maintain regulatory binders and study files; Monitor and report adverse events and protocol deviations; Coordinate study visits and procedures; Track study progress and enrollment; Serve as point of contact for sponsors and monitors.
Seniority
Mid-level, hands-on IC
