Quality Assurance/Regulatory Affairs Coordinator - (Springfield, MO)

Under administrative direction this position will assists with the development, implementation, management, and continual improvement of an effective Quality Assurance (QA)/Regulatory Affairs program. The position is part-time, up to 29 hours per week. Some flexibility with hours is possible. This position serves as a regulatory resource for investigators, clients, and co-workers with an extensive understanding of human subject research regulations and federal guidance documents. Provides consistency and regulatory ability in addition to administrative support to the Bio-Kinetic Institutional Review Board (IRB), serving as a liaison between the IRB and the research team. Work is done in accordance with the processes and procedures that ensure compliance with applicable rules and regulations relative to human subjects in research. Required functions Promote organization's growth and adherence to industry standards in regard to quality assurance and regulatory compliance