Sylvia Webb

Background

About Sylvia Webb

Experienced regulatory submission publisher Many years of experience from pharmaceutical industry working with administration and data systems in different areas within Research and Development, such as Regulatory Affairs, Clinical Development and Discovery. Last 7 years worked with electronic submissions (eCTD), ISI Toolbox, system administration, support and training users in a global document management system (documentum based system). Technical quality control of documentation. Interpret health authority documentation requirements. Functional rep. in global cross functional teams (process- and project teams). Representing my skill in drug project teams and being responsible for ensuring delivery, compliance of standards, project planning and resource estimation. Also worked in the Discovery area in a global group for submission specialists supporting users in Sweden, UK, US, Canada and India. Currently working with medical administration at Karolinska Universitetssjukhuset.