Director, Regulatory Services, Scripps Office for the Protection of Research Subjects Clinical Research Services
For more than 35 years, Ms. Bigby has been involved in clinical research as investigator, research associate, study coordinator, and IRB professional. For the past 14 years, her focus has been on research ethics, protection of human subjects, and regulatory affairs. She is an active member of Public Responsibility in Medicine & Research (PRIM&R) and is serving a 3-year term on the Council for Certified IRB Professionals. She taught Human Subjects Protection and IRBs at the UCSD Extension from 2002-2010 and currently teaches Human Subjects Protection & IRBs at the Clinical Trial Statistics, Design & Execution course for CTSA trainees.