Sarah Roberts has extensive work experience in the regulatory affairs field. Sarah started their career as a Harvard Research Fellow at the Dana Farber Cancer Institute in 1997. Sarah later worked as a Scientist at the Gray Cancer Institute from 1998 to 2002. From 2002 to 2006, Sarah served as a Senior Consultant in Regulatory Affairs at MDS Pharma Services. Sarah then became the Managing Director of Smart Regulatory Solutions Ltd from 2006 to 2007. Sarah joined Celerion (formerly MDS Pharma Services) as a Senior Director of Regulatory Affairs from 2007 to 2011. In 2011, they briefly owned their own company, Smart Regulatory Solutions. Sarah worked at PPD as Director of Global Regulatory Affairs Consulting in 2012 and then joined PRA International as the Executive Director of Global Regulatory Affairs from 2013 to 2014. Sarah held the role of Vice President and Head of Global Regulatory Affairs at ICON plc starting in 2014. Alongside their positions at various companies, Sarah also held leadership roles at TOPRA, including serving as the Chair of the Clinical Trial SPIN and as President.
Sarah Roberts earned a Bachelor of Science (Hons) degree in Pathobiology with Subsidiary Chemistry from the University of Reading in 1993. Sarah went on to pursue a Master of Science (MSc) degree in Toxicology at the University of Surrey from 1993 to 1994. In 1994, they completed their PhD in Pharmacognosy from The School of Pharmacy, University of London. Sarah then obtained an MBA degree in Regulatory Strategy from Henley Business School, where they studied from 2010 to 2013. Sarah also holds the certification of RAC (US) from RAPS, although the specific time of obtaining this certification is not stated.
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