- Evaluate and build relationships with over 1,000-member institutions including the on-boarding of over 300 new institutions signing onto the SMART IRB Agreement.- Advise research teams and IRB/Human Research Protections staff on the SMART IRB platforms, SMART IRB resources and provide regulatory guidance related to the implementation of Single IRB review. - Design and deliver trainings sessions, materials and communications on Single IRB review and SMART IRB resources and systems for IRB/Human Research Protections staff, IRB members, investigators, research staff and SMART IRB Ambassadors. - Evaluate and oversee updates of two online platforms to ensure compliance with human subject regulations and IRB processes. - Collaborate with legal counsel and leadership to strategize and implement necessary changes to the existing SMART IRB reliance agreement.- Oversee and support team meetings and project, including monitoring project milestones, analysis of metrics and reporting of results.

•Manage and track portfolio of 150 oncology research protocols conducted within the Harvard Cancer Center.•Perform regulatory analysis and administrative review of IRB submissions. •Served as an IRB member responsible for IRB reviews and to transcribe complex meeting minutes.•Developed single IRB policies and procedures. •Initiated IRB reliance agreements and managed protocols relying on external IRBs. •Advise and educate study teams on IRB policies and requests.

•Coordinate 3 annual conferences, including: registration, website, CME/CEU credit application, speaker arrangements & hotel rooming/catering/meeting rooms.•Provide support for the Northern New England Perinatal Quality Improvement Network (NNEPQIN) – website upkeep, conduct/compile surveys and evaluations, attend planning committee meetings and distribute information to members. •Perform daily data checks of OBNet database (database is used to collect information on all births for birth certificates and to transmit data to Vital Statistics). •Run reports and queries of database using Crystal Reports for use in quality improvement projects for the department.•Coordinate Research Study – prepare IRB paperwork, compile data & follow up with study providers.

•Perform data entry and triage of human research proposals for review by the IRB.•Invoice and process payments from Industry sponsors. •Update and monitor training database, including updating website.•Generate reports and send monthly reminders for pending items.