Job Abstract
Under limited supervision, coordinates the RIAO Research Program, including clinical trial regulatory affairs and clinical trial and research data coordination. Essential Functions include: Prepares regulatory documents and monitors regulatory activities for assigned clinical trials. Prepares protocol for initial and annual IRB (Institutional Review Board); submits protocol revisions and amendments for IRB review; submits Serious Adverse Events reports and Investigational Drug Safety Reports to ...
Search Terms: Program Coordinator, Research, Clinical Research, Coordinator, Monitoring