Research Regulatory Specialist

Job description

Welcome! We’re excited you’re considering an opportunity with us! To apply to this position and be considered, click the Apply button located above this message and complete the application in full. Below, you’ll find other important information about this position. Examines, evaluates, and investigates conformity with the regulatory and billing aspects of industry and government sponsored clinical trials and investigator-initiated clinical research. This includes securing Institutional Review Board (IRB) approval and maintaining all records pertaining to IRB approval and oversight. Performs various duties, such as research, analysis and auditing in support of projects to assure compliance across all aspects of the research studies. MINIMUM QUALIFICATIONS: EDUCATION, CERTIFICATION, AND/OR LICENSURE: 1. Master's degree OR; Bachelor’s degree AND Three years of experience in regulatory and research patient billing aspects of industry and government sponsored clinical trials including IRB application submissions OR ; Associate’s degree AND Five years of experience in regulatory and research patient billing aspects of industry and government sponsored clinical trials including IRB appli...