Sharon Goldfarb has been working in the medical device fields of regulatory affairs, clinical trials, quality assurance and marketing since the turn of the century. With 18 years of experience, Sharon has worked with medical devices from several different disciplines of medicine helping various companies build and implement studies from the pre-clinical phase through the full blown clinical investigations and subsequent regulatory processes.
Sharon’s career has spanned several companies such as Medinol Ltd., Sightline Technologies (subsequently purchased by Stryker GI), ES Vascular Ltd., and GI View Ltd. During the course of her career, Sharon has worked at all the various positions in the clinical world such as; data input, clinical study monitoring, study coordinator, study manager, medical writer, CRF designer, eCRF builder and co-author of publications. She managed all of these aspects as well as the clinical and regulatory strategy for several companies. Today, Sharon works for SGConsulting as a free-lance consultant for regulatory, clinical affairs for small start-up medical device companies.