JOB SUMMARY: The Clinical Research Study Coordinator executes and coordinates daily clinical research activities according to GCP and FDA/ICH guidelines; completes and organizes all IRB/Sponsor regulatory documents; ensures IRB approved protocols are implemented and followed; conducts study specific training on new or amended protocols; educates patients and their families about clinical trial treatments; identifies patients for study eligibility; executes and documents the informed consent process; monitors patient status and safety; coordinates patient visits according to protocol; collects, processes and ships lab samples; collects, organizes and reports research data and resolves queries; maintains investigational product inventory and oversees the dispensing of investigational product; invoices for study related activities; participates in monitoring visits with study sponsors and regulatory agencies, and reports regularly to the Principal Investigator and Director of Clinical Research.