Bailey Walton Email & Phone Number

Kansas City, MO, US

United States

• Perform regulatory reviews of social/behavioral/educational and biomedical research protocols
• Review and issue exempt and not human subjects research determinations
• Communicate IRB and administrative determinations to researchers
• Liaise with and provide regulatory expertise to study teams and IRB members to facilitate IRB review processes
• Organized a weekly CIP study group
• Edit and provide feedback on study materials (informed consent forms, surveys, etc. to enhance… Show more

Kansas City Metropolitan Area

• Developed a support network of over 5000 Kansas City metro-wide community members and organizations interested in offering or obtaining aid and assistance in the wake of the COVID-19 Pandemic
• Raised funds to provide direct material aid resources to community members and support community programs
• Organized community film screenings, free meals, and discussion events around social justice issues
• Lead organizer of Feedin Folks (preparation/delivery of hot meals), container garden… Show more
• Lead organizer of Feedin Folks (preparation/delivery of hot meals), container garden giveaway, community garden, and the Kansas City Mutual Aid Free Skool (accessible, pay-what-you-can workshops for creative and.
• Panelist at KC Farm School’s 2020 “Let’s Grow!” conference

Las Vegas, Nevada, United States

• Performed initial regulatory reviews of complex social/behavioral/educational and biomedical research protocols, including FDA-regulated research, clinical trials, and research involving vulnerable populations
• Reviewed and issued exempt and not human subjects research determinations
• Co-created an innovative IRB application designed to better assist stakeholders through the IRB process and improve regulatory compliance
• Assisted in the development of policies, forms and processes… Show more
• Assisted in the development of policies, forms and processes managed by the IRB office
• Provided support and mentorship to junior administrators

• Performed initial regulatory reviews of complex biomedical research protocols, including FDA-regulated research, clinical trials, and research involving children
• Provided regulatory, ancillary review, and policy guidance to research stakeholders
• Prepared pre- & post-review materials (reviewer notes, determination letters, minutes)
• Assisted in the development of policies, forms and processes related to the review of activities by the Office of Research Integrity
• Reviewed… Show more
• Reviewed and issued exempt, QI and Not Human Subjects Research determinations

Kansas City, Missouri, United States

• Performed Research Compliance Specialist duties listed below
• Provided education, training and support for research stakeholders such as IRB members, faculty researchers and students
• Conducted select IRB reviews and served as an alternate IRB member
• Trained Research Compliance Specialists in regulatory and administrative duties
• Assisted in developing policies, forms and processes related to activities reviewed by the Office of Research Services and IRB

Kansas City, Missouri Area

• Performed initial regulatory reviews of complex SBE and biomedical research protocols, including FDA-regulated research, clinical trials, and research involving vulnerable populations
• Liaised with and provided regulatory and institutional policy guidance to study teams, the IRB, and other research stakeholders to facilitate the IRB review process
• Reviewed and issued exempt, QI and Not Human Subjects Research determinations
• Facilitated reliance agreements for collaborative and… Show more
• Facilitated reliance agreements for collaborative and multi-site research
• Prepared pre- and post-meeting materials (agendas, minutes, determination letters)

Kansas City, Missouri Area

• Performed the Work Study duties listed below
• Provided assistance to study teams on general and technical issues and routed correspondence to the appropriate compliance staff as needed
• Screened new IRB reliance submissions to ensure all necessary materials were included

Kansas City, Missouri Area

• Provided general office support, including copying, scanning, and filing for the Office of Research Compliance (IRB, RSC, IBC and IACUC)
• Performed pre-reviews to ensure all documentation is included in the IRB application
• Organized catering and room reservations for compliance committee meetings

• Member of a 1-year advisory group comprised of 10 traditional music and dance community members aimed at improving cultural equity within the organization and country song and dance community at large
• Analyzed internal and public-facing materials related to CDSS operations/programming
• Conducted interviews with CDSS board members and staff
• Provided specific recommendations for improving equity and diversity within CDSS
• Contributed to the development of an action plan… Show more
• Contributed to the development of an action plan presented to the Board of Directors Show less

Kansas City, MO

• Provided IRB administrative services for NCI Community Oncology Research Program
• Reviewed research involving Human Subjects for regulatory and policy compliance
• Liaised with study team and IRB members to facilitate IRB review processes
• Prepared and distributed pre- and post-meeting materials
• Trained research study coordinator and the IRB on 2018 revisions to the Common Rule
• Primary contact and facilitator for a successful FDA audit Performed IRB management duties… Show more

Master Of Public Administration - Mpa

Bachelor Of Arts (B.A.), Psychology

Education record