Sharon Trombley

Sharon Trombley is a Senior Associate in Regulatory at Lachman Consultant Services with vast experience in medical technology, regulatory affairs, clinical trials, and document specialist roles. During their time at MMS, Sharon held the position of Senior Regulatory Operations Specialist II. Prior to this, Sharon worked at QuatRx as an Operations Assistant focusing on document specialist tasks, and at Pfizer as a Senior Document Specialist managing various documents for drug submissions. Sharon has a strong background in publishing regulatory submissions and ensuring compliance with standards such as ICH eCTD format.