Sarah Milner
Regulatory Affairs Practice – Europe
OVERVIEW
FOCUS AREA
More than 15 years of experience leading and preparing high-quality regulatory documentation for the pharmaceutical industry.
Leadership of global CTD dossier preparation
Resource management
Development and implementation of quality and regulatory standard for medical writing
Strategic messaging for regulatory submissions
Document quality management
Operational efficiencies
As Director of Medical Writing at ELIQUENT Life Sciences, Sarah Milner leads the company’s clinical authoring team. Her collaboration with ELIQUENT’s team of regulatory experts ensures timely authoring of high quality, strategically-messaged, compliant documents.
Sarah brings more than 15 years of extensive technical writing experience to her role at ELIQUENT Life Sciences. Prior to joining ELIQUENT Life Sciences, Sarah led global medical writing activities and authored documents across a range of therapeutic areas and regions in both a pharmaceutical and CRO environment.
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EDUCATION:
Ph.D in Cell and Molecular Biosciences, University of Newcastle-upon-Tyne
Bachelor of Science (Hons) in Biomedical Sciences, University of Newcastle-upon-TyneASSOCIATION:
EMWA, Associate Editor, Guest Editor, ESS and EDG Leader -
PTC Therapeutics – Director, Medical Writing
Synchrogenix (a Certara company) – Associate Principal Writer and Team Lead
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