-Processes complex IRB submissions (biomedical and social/behavioral human research studies), including conducting regulatory pre-reviews of human research studies to ensure regulatory and institutional compliance.

-Exercises independent judgement in the determination for regulatory requirements.

- Communicates with researchers and research staff to address questions/concerns; provides technical and regulatory support and guidance as needed.

-Provides technical and regulatory support and guidance to researchers and research staff; ensures all WCM institutional requirements are addressed/complete.

-Prepares IRB meeting agendas, attends IRB meetings, generates correspondence/regulatory documents from meetings and drafts meeting minutes in accordance with federal regulatory requirements.

-Works closely with IRB members (WCM faculty and unaffiliated members) to address respective research review concerns and serve as liaison between members and researchers.

-Conducts outreach efforts (training, regulatory guidance, etc.) with assigned WCM departments and/or divisions, and serves as the primary point of contact.

-Serves as a non-supervisory backup for regulatory managers, as needed. For example, administers board meetings and ensures meeting agendas meet regulatory requirements, etc.

-Serves on internal subcommittees, e.g. policy subcommittee, process improvement, etc. to assist with building the WCM HRPP.

-Maintains a current and working knowledge of federal, state and local regulations and institutional policy and procedures to ensure the WCM IRBs and HRPP are in compliance with applicable mandates.

-Performs other related duties as assigned.