Usha Ramesh Pmp

Usha Ramesh, PhD, PMP has a diverse and extensive work experience in the pharmaceutical industry. Usha is currently serving as the Vice President of QA and Regulatory Affairs CMC at Summit Therapeutics, Inc. Prior to this, they worked at Gilead Sciences as the Executive Director of Regulatory Affairs CMC. Usha also held multiple roles at Pharmacyclics, an AbbVie Company, including Executive Director of CMC Regulatory Affairs and Ad. Promo, Executive Director of Regulatory Affairs CMC, Senior Director of Regulatory Affairs, and Director of Regulatory Affairs. Before that, they worked as a Senior Program Manager and Regulatory Consultant at Affymax. Usha also has experience as a Pharmaceutical Industry Consultant and as a Senior Director of Project Management and Product Development at Teikoku Pharma USA. Usha began their career as a Project Leader at Rigel Pharmaceuticals Inc. and as a Senior Scientist and Group Leader at affymax and GlaxoWellcome, respectively. Usha Ramesh holds a PhD and PMP certification.

Usha Ramesh PhD. PMP holds a Certificate in Regulatory Affairs and a Certificate in Clinical Trials Design and Management, both obtained from the University of California, Santa Cruz in 2006-2007. Additionally, Usha Ramesh holds a PhD in Organic Chemistry from Michigan State University and an M.Sc in Organic Chemistry and a B.Sc in Physics, Chemistry, and Math from the University of Mumbai.