Ellen Lane

Ellen Lane is a Clinical Documentation Specialist at Emmes, with experience since October 2013 focusing on quality control and maintenance of Trial Master Files. Prior to this role, Ellen worked at GlaxoSmithKline (formerly Human Genome Sciences, Inc.) from August 2000 to April 2013 as a Regulatory Affairs, Essential Record Documentation Supervisor, managing daily operations of regulatory and clinical records for clinical trials. Ellen began a career in the pharmaceutical industry at Otsuka America Pharmaceutical, Inc. from February 1994 to August 2000, first in an administrative capacity supporting clinical research and later advancing to a QA Manufacturing Documentation Specialist position, overseeing compliance with cGMP and company policies. Ellen holds a Bachelor of Science degree from the University of Maryland.