Strategic guidance from
proven professionals

Elizabeth (Liz) Moore M.S., R.A.C.

Senior Consultant, Clinical Development & Regulatory Affairs

Elizabeth has over 31 years of drug development experience including clinical, regulatory, medical writing, and training in sponsor and CRO companies.  She has managed clinical research associates, regulatory affairs staff, clinical trial assistants, training staff, medical writers, and project managers.  She has over sixteen years of global and domestic project management and study oversight of drug development Phases I-IV, including managing INDs and NDAs as well as device studies.  Therapeutic area experience includes cardiovascular, pulmonary, neurology, gastroenterology, and sickle cell disease.


  • Master of Science, Zoology
    • North Carolina State University, Raleigh, NC
  • Bachelor of Science, Zoology
    • University of North Carolina at Chapel Hill, Chapel Hill, NC


  • Regulatory Affairs Certification