Scott has more than 12 years of experience supporting a diverse client base in the biotechnology and pharmaceutical industries, from start-ups to Fortune 100 companies. Scott’s current focus is assisting small “emerging” companies that are pre-commercial or recently commercialized, in becoming regulatory complaint. Scott’s experience includes leading internal and external audits, process improvement/streamlining, computer systems validation, establishing Quality Management Systems, and regulatory gap assessments.
With over 15 years in the IT industry, prior to making the switch to biotech/pharma, Scott is easily able to get up to speed on new technologies.  He has worked on implementing a range of cloud based and on-premise software systems including; eCTD/submissions, CTMS, eTMF, SAS, IRT, EDC, LMS, DocuSign, medical imaging, network infrastructure, backup/restore,  and track & trace (for commercialized product).
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