Cincinnati, Ohio30+ days ago
Responsibilities : Assist with study participant screening, admission, orientation, conduct, and discharge; Demonstrate technical skills in phlebotomy, laboratory specimen collection, electrocardiogram placement, vital signs, and other protocol-related procedures; Assess, document, and notify appropriate project team members of study participant adverse events in timely manner; Assist other clinical staff with study-related duties (e.g., laboratory draws, electronic data capture entry, queries, follow-up appointments); and. May coordinate studies including working with the research team on development of overall study processes in accordance with the protocol, obtain informed consent, conduct study visits, maintain accurate investigational drug accountability when dispensing study drug.