Dara Dary

Background

About Dara Dary

Manage IRB work activities. • Educate research staff and review all research study documentations. • Monitor and adhere to rules and regulations within Central DuPage Hospital (CDH) system in strict compliance with the study protocols and all CDH policies, as well as, state and federal regulations. • Instrumental in writing and producing manual to assist Research Coordinators in their responsibilities; maintain IRB form revisions; instituted monthly updated email to all Research Coordinators on offices’ new initiatives. • Produce and assist in education segments for the department’s quarterly newsletter. • Manage, update and maintain Office of Research Support (ORS) Team website and IRB members’ website. • Audited and monitored IRB approved studies for Good Clinical Practice (GCP) and International Conference on Harmonisation (ICH) Compliance. • Provide detailed guidance and assistance to new coordinator. • Present professional and friendly presentation and collaboration with colleagues and constituents and Principal Investigator (PI). • Review IRB submissions; study protocol applications, continuing reviews, amendments, and safety reporting. • Attend IRB meetings; generate minutes and letters resulting from the meeting. • Primary contact person for IRB members. • Assist in day-to-day IRB operations since September 2011.