Prior to consulting, Dr. Weinberger was employed by Pacira Pharmaceuticals, Inc. (formerly SkyePharma Inc.) in San Diego, California, as a Senior Regulatory Affairs Associate. While there, she gained experience in international regulatory affairs for both commercial- and development-stage products, and performed technical writing for CMC and clinical submissions. Also in San Diego, Dr. Weinberger was a bench chemist for Adaptive Therapeutics, Inc., a start-up biotech company focused on the discovery and development of peptide-based antibiotics.

Dr. Weinberger received a Ph.D. in Chemistry from Northwestern University and a B.S. in Chemistry from Harvey Mudd College. Her graduate research focused on the synthesis and characterization of metal-conducting polymer composite materials, as well as the preparation of nano-scale materials using atomic force microscopy techniques. Dr. Weinberger was an NIH postdoctoral fellow at the Scripps Research Institute and performed research in the areas of biomimetic peptide catalysts and peptide antibiotics. Dr. Weinberger is the author or co-author of numerous peer-reviewed publications and patents.

As a Scientific and Regulatory Consultant at CBR International, Dr. Weinberger has expanded the company expertise in the areas of chemistry, technical writing, and regulatory affairs. Dr. Weinberger’s expertise and attention to detail ensure the highest quality technical documents and regulatory submissions.

Consistent, thorough and up-to-date analysis of your evolving needs is just the beginning of our commitment to your program. For a comprehensive assessment of your program requirements, please contact us by calling (720) 746-1190 or by email at info@cbrintl.com.