Clinical Research Coordinator 253456

Participant Recruitment & Retention: Identifies, screens, and recruits eligible subjects; obtains informed consent.Study Coordination: Schedules patient visits, conducts study procedures, and ensures protocol adherence.Data Management: Collects, records, and manages source data; completes Case Report Forms (CRFs) and resolves queries.Regulatory Compliance: Maintains regulatory binders, submits documents to IRB, and reports adverse events.Lab/Specimen Processing: Collects, processes, and ships laboratory samples.Investigational Product Management: Manages storage, dispensing, and tracking of study medication/devices.