Qualifications
Bachelor’s Degree
Must have a minimum of 3 years of Clinical Research Coordinator experience working on a drug or device studies
Experience with protocols, patient recruitment, and EDC / EMR Oncology preferred but Cardiology / Neurology are acceptable
Schedule
Must be onsite Monday-Friday Day shift
Clinical Research Coordinator III
Collaborating with nursing staff and Principal Investigator (PI) ascertains pretreatment & eligibility requirements
Interviews participants & obtains social & medical histories; based on results determines & registers participants with appropriate sponsors
Completes informed consent; determines & organizes patient's treatment and test schedules
Manages conduct of experimental tests & procedures
Manages daily operations of a biomedical & / or social-behavioral research study involving multidisciplinary teams of colleagues, sponsors & other external
project stakeholders
Monitors study performance, analyzes & review results, & supervises development & implementation of new protocols
Closely monitors & documents patient's adverse events; partners with nursing staff in modifying dosages, tests & treatment schedule
Manages project data including processing, accuracy, analysis & evaluation of data ensuring that results meet project information and deliverable objectives
Partners with internal / external project and IT staff to create, review, analyze, interpret, summarize and prepare progress & final reports
Manages project, collaborating and partnering with all internal / external staff including sponsoring agencies, organizations & / or other research & / or educational institutions to ensure project objectives and timelines are attained
Additional duties as assigned
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