Position Summary:

• Coordinate and administer protocols and translate protocols into operational implementation and conduct at the foreign, domestic and Rutgers sites.
• Report adverse effects (AEs) to Principal Investigator(s), Regulatory Coordinator, Institutional Review Board (IRB) & Study Sponsor.
• Provide specialized protocol, procedure and application (REDCap, FreezerPro specimen tracking) training to international site study team (investigators and staff).
• Provide visit specific case report forms, receives and reviews study needs.
• Assures timely responses to study inquiries and schedules regular
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  About Rutgers University

  Rutgers, The State University of New Jersey, is a leading national public research university and the state's preeminent, comprehensive public institution of higher education. Rutgers is dedicated to teaching that meets the highest standards of excellence; to conducting research that breaks new ground; and to turning knowledge into solutions for local, national, and global communities. As it was at our founding in 1766, the heart of our mission is preparing students to become productive members of society and good citizens of the world. Rutgers teaches across the full educational spectrum: preschool to precollege; undergraduate to graduate and postdoctoral; and continuing education for professional and personal advancement. Rutgers is New Jersey's land-grant institution and one of the nation's foremost research universities, and as such, we educate, make discoveries, serve as an engine of economic growth, and generate ideas for improving people's lives.

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